http://identifiers.org/hco/11/GRCh38#100687399-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#9238956-C-A

http://identifiers.org/hco/11/GRCh38#100687577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9238838-C-A

100687577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9238838-C-T

100687584-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9238831-T-A

100687584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9238831-T-C

100687597-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9238818-G-C

100687600-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9238815-C-G

100687600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9238815-C-T

100687937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 9238540-G-A

100687937-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 9238540-G-T

100687980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9238498-A-G

100688050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9238427-G-A

100688050-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9238427-G-T

100688079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9238386-T-C

100688079-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9238386-T-G

100688152-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9238281-G-T

100688355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9237997-A-G

100688411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9237937-T-C

100688481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9237870-T-C

http://identifiers.org/hco/11/GRCh38#100688562-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9237835-A-C

100689802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9236716-G-T

100692088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9233278-A-G

100692125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9233241-T-C

100692227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9233142-A-G

100692244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9233125-C-T

100692465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9232127-A-G

100692467-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9232125-T-A

100692519-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, undefined
orthologous variants: 9232089-C-G

100693291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9230128-A-G

100693548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9229889-C-T

100693564-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9229873-T-A

100693636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9229808-G-A

100693654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9229786-T-C

100693744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9229693-G-A

100693823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9229613-T-C

http://identifiers.org/hco/11/GRCh38#100694291-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9229475-C-A

100694336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9229433-T-C

100694369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9229386-G-A

100694415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9229340-A-G

100694455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9229300-G-A

100694695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9229072-C-T

100695105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9228988-T-C

100695127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9228969-A-G

100703788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9227357-C-T

100703797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9227348-C-T

100703947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9227191-C-T

100704049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9226938-G-A

100704169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9226835-G-A

100704182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9226822-C-T

100704506-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9226471-C-G

100704506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9226471-C-T

100705059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9226081-A-G

100705059-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9226081-A-T

100705075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9226065-G-T

100705093-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9226047-G-C

100705093-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9226047-G-T

100705277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9225876-A-G

100705278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9225875-T-C

100705587-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9225382-T-A

100706404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9225277-T-C

100706404-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9225277-T-G

100706509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9225171-A-G

http://identifiers.org/hco/11/GRCh38#100706777-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9224148-A-C

100706824-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9224108-T-A

100709729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9223802-T-C

100709804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9223736-C-T

100710063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9223492-C-T

100710144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9223417-T-C

100712579-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9222239-G-C

100712659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9222138-G-A

100712671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9222126-G-A

100712743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9222052-G-A

100713054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9221765-T-C

100713170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9221654-A-G

100713185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9221639-G-A

100713242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9221566-C-T

100713760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9220805-A-G

100713767-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9220799-G-T

100713926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9220638-G-A

http://identifiers.org/hco/11/GRCh38#100713995-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9220573-A-C

100714523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9220065-G-A

100714706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9219382-A-G

100715099-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9219323-G-T

100715316-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9219129-G-C

100715320-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9219125-T-G

100715377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9219083-G-A

100715991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9218687-G-A

100715992-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9218686-C-G

100716123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9218596-C-T

100716153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9218566-C-T

100716399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9218346-A-G

100716487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9218259-T-C

100716506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9218240-T-C

100716753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9218052-A-G

100716757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9218048-T-C

100718288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9217009-G-A

100718409-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9216888-T-A

http://identifiers.org/hco/11/GRCh38#100718500-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9216799-A-C

100718509-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9216786-C-G

100718529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9216758-A-G

100718619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9216668-A-G

100719247-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9215256-T-A

100719622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9214895-C-T

100719671-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9214849-T-G

100719681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9214833-G-A

100719858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9214677-C-T

100720685-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9213565-T-G

100721086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9213252-A-G

100730467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9211518-C-T

100732563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9209443-A-G

100732782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9209273-C-T

http://identifiers.org/hco/11/GRCh38#100732794-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9209259-A-C

100732962-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9209099-A-T

100733155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9208940-T-C

100733274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9208878-A-G

100737777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 9205245-T-C

100737998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 9204859-C-T

100738019-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 9204838-T-A

100738019-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 9204838-T-G

100738235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 9204625-C-T

100738595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9203307-A-G

100738704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9203208-T-C

100738973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9202960-G-A

100739109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9202829-G-A

100739332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9202450-T-C

100739459-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9201493-G-T

100739556-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9201395-T-C

100739556-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9201395-T-G

100739582-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9201369-C-G

100739651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9201310-A-G

100739743-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9201155-T-A

100740343-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9200229-T-G

http://identifiers.org/hco/11/GRCh38#100740672-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9200008-C-A

100740672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9200008-C-T

100740797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9199901-C-T

100741895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9198932-G-A

100742090-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9198720-T-A

100754214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9191613-G-A

100754237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9191629-T-C

100754595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9192791-G-A

100754595-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9192791-G-T

100754640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9192835-C-T

100754890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9193058-C-T

http://identifiers.org/hco/11/GRCh38#100754969-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9193130-C-A

100754969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9193130-C-T

100756345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9194331-C-T

100756350-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9194336-A-T

100756547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9194506-C-T

http://identifiers.org/hco/11/GRCh38#100756666-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9194625-C-A

100756666-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9194625-C-G

100756696-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9194655-T-A

100756696-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9194655-T-G

http://identifiers.org/hco/11/GRCh38#100756791-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9194745-A-C

100756798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9194751-A-G

100757071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9194951-G-A

100757222-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9195601-T-A

100757243-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9195620-C-G

100757384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9195759-C-T

http://identifiers.org/hco/11/GRCh38#100757500-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9195871-A-C

100757601-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9195967-G-C

100757628-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9195994-T-A

100757941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9196316-G-A

100758018-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9196395-C-G

100758391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9197766-A-G

http://identifiers.org/hco/11/GRCh38#100758468-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9197822-A-C

100758482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9197836-A-G

100759195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9190692-G-A

100759309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9190586-C-T

100759363-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9190529-T-A

http://identifiers.org/hco/11/GRCh38#100759414-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9190478-C-A

100759618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9190301-A-G

100759628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9190291-A-G

100760727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9189640-C-T

100760754-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9189606-A-G

100761431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9189173-T-C

100761741-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9188858-T-G

100762151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9188582-G-A

100762358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9188381-G-A

100762629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9188152-G-A

100765133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9186929-A-G

100765133-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9186929-A-T

100765245-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9186819-C-G

100765322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9186751-A-G

100765395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9186692-C-T

100765396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9186691-G-A

100765401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9186686-G-A

100765538-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9186331-G-C

100765840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9185637-A-G

http://identifiers.org/hco/11/GRCh38#100765847-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9185632-A-C

100765860-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9185619-G-T

100765960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9185531-G-T

100765978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9185513-T-C

100765978-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9185513-T-G

100766023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9185462-A-G

100766061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9185424-C-T

100766810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9184136-A-G

100767081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9183879-C-T

100767091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9183869-T-C

100767092-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9183868-T-G

100767189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9183788-A-G

http://identifiers.org/hco/11/GRCh38#100767381-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9182654-A-C

100767418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9182617-G-A

100767436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9182594-A-G

http://identifiers.org/hco/11/GRCh38#100767500-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9182534-A-C

100767502-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9182532-A-T

100767536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9182502-A-G

100767536-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9182502-A-T

100767550-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9182490-A-T

100767577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9182462-G-A

100768169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9181483-A-G

http://identifiers.org/hco/11/GRCh38#100768218-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9181445-A-C

http://identifiers.org/hco/11/GRCh38#100769414-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9180671-A-C

100769414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9180671-A-G

100770005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9180352-G-T

http://identifiers.org/hco/11/GRCh38#100770259-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9180184-A-C

100770299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9180159-T-C

100770444-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9180020-T-A

100770444-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9180020-T-G

100770515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9179947-T-C

100770540-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9179922-T-A

100770564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9179898-T-C

100770564-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9179898-T-G

100773171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9178344-A-G

100773336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9178219-A-G

http://identifiers.org/hco/11/GRCh38#100773523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9178034-C-A

http://identifiers.org/hco/11/GRCh38#100773928-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9177640-A-C

100774205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9177352-C-T

100774238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9177319-A-G

100774239-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9177318-A-T

100774292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9177269-C-T

100774378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9177171-C-T

100774547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9176878-T-C

100774559-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9176863-G-C

100774788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9176625-G-A

100774807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9176618-G-A

100774821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9176604-A-G

100774939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9176503-G-A

100775146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9176321-T-C

100775146-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9176321-T-G

100775497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9176010-G-A

100775505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9176002-A-G

100775526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9175981-A-G

100775758-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9175755-G-C

100775766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9175747-A-G

100776366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9175276-G-A

100776477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9175171-G-A

100776611-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9175039-G-C

100776648-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9175001-C-G

100776650-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9174999-G-C

100777097-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9174861-T-A

100777313-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9174350-C-G

100777357-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9174305-G-T

100778395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9173363-A-G

100778998-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9172610-T-G

100779048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9172560-T-C

100779156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9172458-A-G

100779215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9172400-G-A

100779215-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9172400-G-C

100779223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9172392-G-A

100779223-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9172392-G-T

100780093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9172179-T-C

100780200-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9172060-G-T

100780244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9172020-C-T

100780375-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9171903-A-T

http://identifiers.org/hco/11/GRCh38#100780527-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9171763-C-A

100780885-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9171402-G-C

100782539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9169224-C-T

100782567-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9169204-T-G

100782698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9169096-T-C

100782742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9169064-G-A

100782742-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9169064-G-C

100782830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9168941-A-G

100782993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9168696-A-G

100784289-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9167350-G-T

100784361-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9167285-C-G

100784365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9167281-A-G

http://identifiers.org/hco/11/GRCh38#100784493-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9167086-A-C

100784507-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9167075-G-C

100784507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9167075-G-T

100784520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9167062-T-C

100784945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9166547-A-G

100784945-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9166547-A-T

100785316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9165984-G-A

100785317-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9165983-G-T

100785716-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9165620-G-T

100785723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9165613-A-G

100785898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9165454-G-A

100785898-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9165454-G-T

100785946-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9165418-G-C

100785976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9165385-G-A

100786217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9165269-C-T

100786232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9165256-G-A

100786238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9165250-C-T

100786466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9165045-T-C

100786490-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9165022-T-G

100786537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9164975-G-A

100786543-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9164969-A-T

100786571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9164945-A-G

http://identifiers.org/hco/11/GRCh38#100787633-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9164099-C-A

100787633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9164099-C-T

100787754-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9164003-G-C

100787976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9163799-G-A

100788647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9162998-C-T

100788681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9162956-G-A

100788681-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9162956-G-T

100788722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9162908-G-A

100788723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9162907-T-C

100788757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9162873-G-A

100788815-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9162815-T-G

100788938-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9162691-T-A

100788938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9162691-T-C

100790236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9162412-A-G

100790287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9162358-T-C

100790346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9162300-T-C

100790426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9162222-T-C

100790474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9162177-T-C

100790666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9161983-T-C

100790675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9161974-G-A

http://identifiers.org/hco/11/GRCh38#100790705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9161942-C-A

100790714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9161933-T-C

100790841-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9161821-T-A

100790904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9161776-G-A

100791097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9161616-A-G

100791097-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9161616-A-T

http://identifiers.org/hco/11/GRCh38#100791349-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#9158329-C-A

100791849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9157850-A-G

100792082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9157633-G-A

100794654-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-C

100794711-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9155700-C-G

100794786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9155638-A-G

100794801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9155623-A-G

100794807-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9155617-A-T

100794937-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9155500-T-A

100794979-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9155476-T-A

100794979-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9155476-T-G

100794983-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9155472-T-A

100794983-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9155472-T-G

http://identifiers.org/hco/11/GRCh38#100795019-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9155451-A-C

100795061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9155407-T-C

100795222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9155247-A-G

100795501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9154958-T-C

100795659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9154799-A-G

100795702-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9154762-C-G

100806665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9153954-T-C

http://identifiers.org/hco/11/GRCh38#100806736-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9153905-A-C

100807772-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9151199-T-G

100807870-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9150695-G-C

100807873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9150692-C-T

100807905-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9150661-C-G

100807975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9150589-T-C

100808266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9150299-A-G

100808354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9150234-T-C

100815294-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9149242-G-T

http://identifiers.org/hco/11/GRCh38#100815380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9149166-C-A

100816241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9146962-T-C

100816396-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9146812-G-C

100816396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9146812-G-T

100816543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9146668-A-G

100816771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9146429-A-G

100816918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9146324-G-A

100816918-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9146324-G-T

100816952-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9146305-G-C

100816952-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9146305-G-T

http://identifiers.org/hco/11/GRCh38#100816959-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9146298-C-A

100817110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9146212-G-A

100817120-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9146205-A-T

100817234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9146111-G-A

100817715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9145702-G-A

http://identifiers.org/hco/11/GRCh38#100817781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9145644-C-A

100822083-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9144673-C-G

http://identifiers.org/hco/11/GRCh38#100822308-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9144308-C-A

100822308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9144308-C-T

http://identifiers.org/hco/11/GRCh38#100822479-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9144155-C-A

100822615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9144022-A-G

100822671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9143967-A-G

100822700-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9143929-A-T

100823078-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9143679-G-T

100823083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9143674-C-T

http://identifiers.org/hco/11/GRCh38#100823231-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9143560-A-C

100823255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9143531-G-A

http://identifiers.org/hco/11/GRCh38#100823481-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9143366-C-A

100823858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9143027-C-T

100823870-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9143015-T-A

100823870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9143015-T-C

100823949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9142956-T-C

100824260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9142673-A-G

100824275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9142658-T-C

100824514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9142418-C-T

100824687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9142286-A-G

100824687-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9142286-A-T

100824757-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9142235-T-A

100824936-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9142080-G-T

100825096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9141913-G-A

100825684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9141015-A-G

http://identifiers.org/hco/11/GRCh38#100825721-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9140979-A-C

100825721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9140979-A-G

100826536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9140072-A-G

100826557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9140051-G-A

http://identifiers.org/hco/11/GRCh38#100826587-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9140032-C-A

100826680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9139943-C-T

100826701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9139922-G-A

100826934-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9139710-G-C

100826969-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9139678-T-G

100826975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9139672-G-A

100827362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9139605-A-G

100827560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9139433-C-T

100830760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9138493-G-A

100831178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9137728-G-A

100831516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9137005-T-C

100831967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9136577-A-G

100831967-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9136577-A-T

100832032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9136512-C-T

100834805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9131689-G-A

100835044-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9131343-T-G

http://identifiers.org/hco/11/GRCh38#100835077-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9131312-A-C

100835191-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9131223-C-G

100835191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9131223-C-T

100835560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9130652-G-A

100835765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9130471-T-C

100835792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9130450-A-G

100835904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9130351-T-C

100840774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9129968-A-G

100841347-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9129411-C-G

100841347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9129411-C-T

100841350-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9129408-G-T

100841417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9129350-G-A

http://identifiers.org/hco/11/GRCh38#100841514-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9129261-C-A

100841542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9129233-C-T

http://identifiers.org/hco/11/GRCh38#100845564-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9127333-C-A

100845564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9127333-C-T

100845565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9127332-G-A

100845565-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9127332-G-C

100845735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9127194-T-C

100845782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9127153-T-C

100845834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9127117-A-G

100845997-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9126977-T-A

100846322-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9126753-C-G

100846395-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9126678-T-A

100846405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9126669-G-A

100846405-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9126669-G-T

100847795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9125665-C-T

100847926-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9125535-A-T

100848269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9125186-G-A

http://identifiers.org/hco/11/GRCh38#100848339-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9125117-A-C

100848344-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9125112-G-C

100848415-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9125028-A-T

100848424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9125019-A-G

100848424-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9125019-A-T

http://identifiers.org/hco/11/GRCh38#100848443-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9124999-C-A

100848867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9124869-G-A

100848922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9124841-G-A

100848922-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9124841-G-T

100848990-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9124791-T-G

100849172-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9124626-T-A

100849380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9124420-A-G

100849774-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9124011-G-T

100851965-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9122480-G-T

100852050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9122419-A-G

100852073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9122400-C-T

100852190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9122298-G-A

100852205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9122283-G-A

100852263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9122225-A-G

100852598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9121853-C-T

100852627-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9121822-A-T

100852659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9121790-G-A

100852659-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9121790-G-T

100852669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9121782-G-A

100852669-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9121782-G-C

100852812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9121642-G-A

100852812-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9121642-G-T

100852950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9121523-G-A

http://identifiers.org/hco/11/GRCh38#100852954-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9121519-A-C

100853420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9121063-T-C

100853454-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9120974-G-T

100854359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9120404-T-C

100854415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9120345-C-T

100854919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9119972-G-A

100854919-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9119972-G-T

100854961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9119929-G-A

100854967-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9119923-G-T

100855348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9119615-A-G

100855565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9119434-G-A

100855571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9119428-A-G

http://identifiers.org/hco/11/GRCh38#100855688-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9119316-A-C

100855770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9119160-T-C

100856025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9118804-A-G

100856067-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9118766-A-T

100856228-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9118594-A-G

100856236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9118586-A-G

100856278-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9118547-T-A

100856297-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9118528-G-T

100856304-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9118521-C-G

100856356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9118471-A-G

100856392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9118435-A-G

100856544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9118289-A-G

100856620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9118223-A-G

http://identifiers.org/hco/11/GRCh38#100856671-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9118171-A-C

100857102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9117788-A-G

100858500-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9116879-T-G

100858614-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9116754-G-T

100858932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9116363-A-G

100859001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9116295-T-C

http://identifiers.org/hco/11/GRCh38#100859324-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9116000-C-A

100859324-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9116000-C-G

100859342-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9115982-T-A

100859342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9115982-T-C

100859342-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9115982-T-G

100859356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 9115958-G-A

100859356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 9115958-G-T

100859362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 9115952-A-G

100859392-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9115922-A-T

100859416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9115899-A-G

100859640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9115674-T-C

100859640-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9115674-T-G

100859669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9115643-T-C

http://identifiers.org/hco/11/GRCh38#100859717-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9115596-C-A

100859717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9115596-C-T

100859748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9115535-C-T

100859799-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9115482-T-A

100859799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9115482-T-C

100859800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9115481-G-A

100859826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9115455-A-G

100859826-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9115455-A-T

100859827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9115454-G-A

100859827-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9115454-G-T

http://identifiers.org/hco/11/GRCh38#100859889-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9115390-C-A

100859889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9115390-C-T

100859972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9115288-G-A

100859990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9115265-T-C

100860333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9114656-T-C

100860333-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9114656-T-G

100860464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9114520-T-C

100860579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9114386-A-G

100860601-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9114364-C-G

100860750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9114211-A-G

100860799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9114161-T-C

100860822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9114147-C-T

http://identifiers.org/hco/11/GRCh38#100862351-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9113809-C-A

100862351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9113809-C-T

100862461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9113697-T-C

100862588-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9113576-A-T

100862604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9113560-G-A

100862637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9113536-T-C

100862651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9113526-A-G

http://identifiers.org/hco/11/GRCh38#100863155-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9113283-A-C

100863517-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9112927-G-T

100863556-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9112887-T-C

http://identifiers.org/hco/11/GRCh38#100863577-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9112866-A-C

100863588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9112853-A-G

100863646-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9112800-G-C

100863843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9112598-C-T

100864030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9112458-T-C

http://identifiers.org/hco/11/GRCh38#100864100-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9112378-C-A

100864143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9112334-A-G

100864165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9112321-A-G

100864714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9111970-A-G

100864775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9111892-T-C

100865052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9111629-G-A

100865129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9111553-G-A

100865152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9111530-A-G

100865206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9111495-A-G

100865242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9111462-A-G

100865262-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9111442-T-C

http://identifiers.org/hco/11/GRCh38#100865263-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9111441-C-A

100865263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9111441-C-T

100865318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9111384-C-T

100865334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9111368-G-A

100869826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9109393-A-G

100872656-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9108556-G-C

100872712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9108493-G-A

100872828-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9108391-G-C

http://identifiers.org/hco/11/GRCh38#100872952-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9108287-A-C

100872987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9108258-C-T

100873008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9108237-G-A

100873133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9107947-C-T

100873147-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9107933-G-C

100873152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9107928-G-A

100873280-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9107813-A-T

100876172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9105733-G-A

100876172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9105733-G-T

100876176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9105729-G-T

100876295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9105613-A-G

100876304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9105604-C-T

100876415-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9105525-G-C

100876894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9105045-T-C

100877096-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9104844-T-G

100877099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9104841-T-C

100877257-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9104679-G-T

100877272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9104665-A-G

100877415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9104530-T-C

100877587-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9104383-G-T

http://identifiers.org/hco/11/GRCh38#100877612-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9104355-A-C

100877612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9104355-A-G

100877634-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9104334-G-C

100879204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9103601-G-T

100879213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9103593-A-G

100879299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9103524-T-C

100879359-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9103463-A-T

100879445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9103345-A-G

100879544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9103218-G-A

100879726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9103050-C-T

100879735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9102907-C-T

100879855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9102788-G-A

http://identifiers.org/hco/11/GRCh38#100879959-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9102691-A-C

100883920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9102247-A-G

100884573-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9101266-T-G

100884749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9101146-C-T

100884920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9100176-A-G

100884968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9100134-G-T

100884980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9100131-G-A

100884980-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9100131-G-C

100885404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9099734-T-C

100885465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9099626-A-G

100885483-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9099577-T-G

100885500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9099516-A-G

100885819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9099214-G-A

100885838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9099184-G-A

100885958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9099075-A-G

100886029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9099009-A-G

100886090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9098962-T-C

100886112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9098941-C-T

http://identifiers.org/hco/11/GRCh38#100888420-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9095978-A-C

http://identifiers.org/hco/11/GRCh38#100888530-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9095854-C-A

100888530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9095854-C-T

http://identifiers.org/hco/11/GRCh38#100888531-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9095853-A-C

100888531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9095853-A-G

100888575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9095809-C-T

100888631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9095756-A-G

100892411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9093783-G-A

100892710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9093489-T-C

100893021-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9093226-C-G

100893021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9093226-C-T

100893094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9093154-C-T

100893189-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9092937-T-G

100893306-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9092821-C-G

http://identifiers.org/hco/11/GRCh38#100893420-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9092648-A-C

100893428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9092640-G-A

100893437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9092631-A-G

100893457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9092552-A-G

http://identifiers.org/hco/11/GRCh38#100893494-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9092350-A-C

100893500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9092344-A-G

100893514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9092330-G-A

100893660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9092134-A-G

100893702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9092091-A-G

100893807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9092004-T-C

100893816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9091995-T-C

100893902-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9091911-C-G

100894065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9091754-T-C

100895514-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9090677-A-T

100895515-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9090676-A-T

http://identifiers.org/hco/11/GRCh38#100895517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9090674-C-A

100895517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9090674-C-T

100903113-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9082665-A-T

100903121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9082657-A-G

100903294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9082486-C-T

100903331-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9082449-T-A

100904681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9081949-T-C

100904804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9081827-A-G

100904804-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9081827-A-T

100904855-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9081790-A-T

100904957-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9081689-T-G

100904989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9081659-T-C

100907146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9080958-C-T

100907298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9080801-A-G

100907300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9080799-A-G

100907345-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9080753-A-T

100907349-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9080750-G-C

100907397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9080701-T-C

100907906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9079884-A-G

100907952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9079821-T-C

100907952-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9079821-T-G

100909871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9078367-G-A

http://identifiers.org/hco/11/GRCh38#100910049-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9078225-A-C

100910049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9078225-A-G

100910229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9078071-T-C

100910243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9078067-C-T

100910345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9077962-T-C

100910674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9077685-G-A

100910770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9077602-G-A

100910780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9077592-T-C

100911174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9077306-C-T

100911278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9077203-C-T

100911731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9077056-C-T

100912560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9076022-T-C

100912635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9075958-A-G

100912674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9075923-A-G

100912788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9075808-G-A

http://identifiers.org/hco/11/GRCh38#100912860-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9075690-C-A

100912860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9075690-C-T

http://identifiers.org/hco/11/GRCh38#100913395-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9075074-C-A

100913395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9075074-C-T

100913407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9075054-G-A

100913407-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9075054-G-T

http://identifiers.org/hco/11/GRCh38#100913542-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9074919-C-A

100913542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, missense_variant
orthologous variants: 9074919-C-T

100913627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9074856-T-C

http://identifiers.org/hco/11/GRCh38#100913628-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9074855-C-A

100913666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9074832-G-A

100913671-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9074827-G-T

http://identifiers.org/hco/11/GRCh38#100913693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9074802-C-A

100914337-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9074451-A-T

100914386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9074398-A-G

100914481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9074303-A-G

100914629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9074137-C-T

100914958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9073640-G-A

100915349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9073170-A-G

100915362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9073157-T-C

http://identifiers.org/hco/11/GRCh38#100915607-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9072968-A-C

100915666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9072901-G-A

100915706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9072857-A-G

100915747-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9072816-C-G

http://identifiers.org/hco/11/GRCh38#100915789-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9072778-A-C

100915804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9072763-A-G

100915820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9072746-A-G

100915846-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9072720-G-C

100915868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9072701-G-A

100915868-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9072701-G-C

100915889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9072680-G-A

100915930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9072640-C-T

100916187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9072411-G-A

http://identifiers.org/hco/11/GRCh38#100916358-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9072205-A-C

100916581-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9072028-T-G

http://identifiers.org/hco/11/GRCh38#100916610-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9071999-C-A

100917913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9071133-C-T

100918016-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9071034-T-G

100918421-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9070301-T-A

100918439-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9070280-C-G

100918494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9070225-G-T

100918562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9070159-A-G

100918573-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9070148-A-T

100918609-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9070112-G-C

100919439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9061406-C-T

100919770-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9061228-T-G

100919826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9061216-G-A

100919826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9061216-G-T

100919868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9061171-G-A

100919950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9061092-C-T

100920103-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9060977-C-G

100920500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9060663-A-G

100920786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9060412-T-C

100920802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9060407-C-T

100920803-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9060406-A-T

100921626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9059027-A-G

http://identifiers.org/hco/11/GRCh38#100921636-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9059017-C-A

100921848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9058841-C-T

100921936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9058768-G-A

100921947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9058757-T-C

100922017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9058702-G-T

100922042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9058689-C-T

http://identifiers.org/hco/11/GRCh38#100922075-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9058656-A-C

100922095-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9058636-G-T

100922426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9058359-G-A

100922474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9058312-G-A

100922787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9054620-A-G

100922847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9054565-G-A

100922966-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9054463-G-C

100923000-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9054429-C-G

100923110-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9054332-A-T

100923133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9054309-G-A

100923252-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9053912-G-T

100923520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9053646-T-C

http://identifiers.org/hco/11/GRCh38#100923543-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9053623-C-A

100923603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9053561-G-A

100923636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9053542-G-A

100923648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9053530-T-C

http://identifiers.org/hco/11/GRCh38#100930561-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9050922-A-C

100930696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9050790-T-C

100930765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9050728-C-T

100930766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9050727-G-A

100931418-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9050585-T-C

100931602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9050410-A-G

100932628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9049604-T-C

100932634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9049598-T-C

100932868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9049265-G-A

100932914-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9049220-G-T

100932927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9049209-A-G

100932997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9049159-C-T

100933114-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9049040-A-T

100933127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9049027-A-G

100933127-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9049027-A-T

100933317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9048791-G-A

100933317-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9048791-G-T

http://identifiers.org/hco/11/GRCh38#100933325-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9048783-A-C

100933325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9048783-A-G

http://identifiers.org/hco/11/GRCh38#100933355-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9048729-A-C

100933355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9048729-A-G

100933385-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9048699-T-A

100933385-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9048699-T-G

100933429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9048659-C-T

100933430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9048658-A-G

100933490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9048618-C-T

100933976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9048415-G-A

100933977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9048414-G-A

100934026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9048393-A-G

100934026-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9048393-A-T

100934027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9048392-T-C

100934038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9048381-C-T

100934239-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9048189-C-G

100934245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9048183-A-G

100934614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9048035-T-C

100934807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9047858-G-A

100934905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9047717-T-C

100935078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9047558-T-C

http://identifiers.org/hco/11/GRCh38#100935104-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9047530-A-C

100935156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9047483-G-A

100935156-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9047483-G-T

http://identifiers.org/hco/11/GRCh38#100935163-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9047476-C-A

100935181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9047458-T-C

100935338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9047297-A-G

http://identifiers.org/hco/11/GRCh38#100935399-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9047232-A-C

100935636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9046871-G-A

100935636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9046871-G-T

100935722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9046817-A-G

100935736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9046803-T-C

100935738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9046801-A-G

100936139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9046697-G-A

100936145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9046691-A-G

100936173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9046663-G-A

100936173-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9046663-G-T

100936203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 9046633-A-G

100936224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: missense variant
orthologous variants: 9046612-A-G

100936412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9045480-T-C

http://identifiers.org/hco/11/GRCh38#100936414-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9045478-C-A

http://identifiers.org/hco/11/GRCh38#100936450-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9045441-C-A

100936451-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9045440-T-A

100936451-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9045440-T-G

http://identifiers.org/hco/11/GRCh38#100936460-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9045431-C-A

100936460-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9045431-C-G

100936460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9045431-C-T

http://identifiers.org/hco/11/GRCh38#100936474-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9045411-A-C

100936474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9045411-A-G

100936667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9045259-C-T

100936682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9045244-T-C

100936798-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9045130-G-T

100936822-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9045102-T-G

100937030-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9044916-C-G

100939571-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9037952-T-A

100939571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9037952-T-C

100939572-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9037951-G-C

100939590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9037933-C-T

100939734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9037796-G-A

100939951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9037594-A-G

100939976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9037580-T-C

100940243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9037309-T-C

100940434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9037120-G-A

100940486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9037076-G-A

100940506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9037056-C-T

100940594-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9036951-G-T

100940652-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9036883-T-A

100940652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9036883-T-C

100941719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9035670-T-C

http://identifiers.org/hco/11/GRCh38#100941723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9035666-C-A

100941723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9035666-C-T

http://identifiers.org/hco/11/GRCh38#100941745-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9035644-A-C

100941853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: missense variant
orthologous variants: 9035539-G-A

100942268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9035135-G-A

100942648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9034576-C-T

100942848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9034381-C-T

100943065-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9034166-T-A

100943065-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9034166-T-G

100943453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9033840-T-C

100943517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9033781-T-C

100943611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9033709-A-G

100943688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9033655-G-A

100943688-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9033655-G-C

100943688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9033655-G-T

http://identifiers.org/hco/11/GRCh38#100943711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9033628-C-A

100943711-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9033628-C-G

100943774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: missense variant
orthologous variants: 9033564-A-G

100943822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: missense variant
orthologous variants: 9033516-G-A

100943822-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: missense variant
orthologous variants: 9033516-G-T

http://identifiers.org/hco/11/GRCh38#100943876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9033462-C-A

100943882-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9033456-T-G

100943885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9033453-T-C

100943916-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9033429-T-A

100943936-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9033409-T-A

100943949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9033393-G-A

100943949-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9033393-G-T

100947808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9031834-T-C

100948083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9031472-C-T

100948122-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9031428-T-A

100948322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9031038-A-G

http://identifiers.org/hco/11/GRCh38#100948326-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9031034-C-A

100948326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9031034-C-T

http://identifiers.org/hco/11/GRCh38#100948339-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9031021-C-A

100948339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9031021-C-T

100948351-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9031014-T-G

http://identifiers.org/hco/11/GRCh38#100948360-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9031005-C-A

100948360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9031005-C-T

100948420-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9030941-A-T

100948427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9030933-T-C

100948434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9030910-A-G

100948571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9030757-T-C

100948580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9030751-T-C

100948593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9030734-T-C

100948593-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9030734-T-G

http://identifiers.org/hco/11/GRCh38#100948612-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9030714-A-C

100948612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9030714-A-G

100948612-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9030714-A-T

100949117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9030299-A-G

100949156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9030264-G-A

100949164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9030256-C-T

100949184-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9030237-C-G

100949710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9029666-G-A

100949787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9029585-G-A

http://identifiers.org/hco/11/GRCh38#100949926-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9029452-C-A

100949926-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: missense variant
orthologous variants: 9029452-C-G

100953566-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9029054-T-A

100953693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9028939-T-C

100953750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9028856-A-G

100953789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9028827-C-T

100953822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9028790-T-C

100953979-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9028650-T-A

100953979-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9028650-T-G

100953982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9028647-T-C

100954023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9028605-A-G

100954085-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9028549-A-T

100954108-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9028542-C-G

100954153-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9028498-C-G

100954506-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9028213-G-C

100954727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9027987-C-T

100954889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9027884-G-A

100954897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9027876-T-C

100955124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9027673-A-G

100955514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9027326-A-G

100955965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9026603-G-A

100956025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9026544-G-A

100956145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9026476-T-C

100956322-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9026287-C-G

100956349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9026260-A-G

100956542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9026117-A-G

100956711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9025945-T-C

100956948-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9025661-C-G

100957536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9019721-G-A

100957536-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9019721-G-T

100957781-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9019495-T-G

http://identifiers.org/hco/11/GRCh38#100957793-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9019485-A-C

100957855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9019431-G-A

100957865-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9019421-T-G

100957925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9019362-T-C

http://identifiers.org/hco/11/GRCh38#100957959-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9019326-A-C

100957984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9019301-C-T

100958030-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9019262-G-C

100958036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9019256-A-G

100958036-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9019256-A-T

100959185-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: intron variant
orthologous variants: 9019059-A-T

100959863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 9018285-G-A

100959863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 9018285-G-T

100960045-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9018045-T-A

100960045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9018045-T-C

100960045-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9018045-T-G

http://identifiers.org/hco/11/GRCh38#100960085-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9017968-C-A

100960085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9017968-C-T

http://identifiers.org/hco/11/GRCh38#100960344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9017597-C-A

100960730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9017221-T-C

100960751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9017200-A-G

100960792-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9017159-G-T

http://identifiers.org/hco/11/GRCh38#100960798-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9017153-C-A

100960818-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9017133-C-G

100960839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9017111-A-G

100961016-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9016934-T-A

100961017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9016933-A-G

100961031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9016917-T-C

100961048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9016900-A-G

http://identifiers.org/hco/11/GRCh38#100961053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9016895-C-A

100961053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9016895-C-T

100961066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9016876-T-C

100961077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9016865-G-A

100961077-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9016865-G-T

http://identifiers.org/hco/11/GRCh38#100961390-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9016535-A-C

100961390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9016535-A-G

100961415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9016510-A-G

http://identifiers.org/hco/11/GRCh38#100961470-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9016475-C-A

100961501-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9016435-T-G

100961651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9016260-C-T

http://identifiers.org/hco/11/GRCh38#100961716-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9016195-A-C

100961716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 9016195-A-G

100961716-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 9016195-A-T

100961801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9016110-G-A

100961801-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9016110-G-T

http://identifiers.org/hco/11/GRCh38#100961817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9016094-C-A

100961817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9016094-C-T

100961822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9016089-G-A

http://identifiers.org/hco/11/GRCh38#100961833-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9016078-A-C

100961833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9016078-A-G

100961845-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9016066-G-T

http://identifiers.org/hco/11/GRCh38#100961850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9016061-C-A

100961850-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9016061-C-G

100961912-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9016003-G-T

100961973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9015955-G-A

100962037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9015890-G-A

100962037-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9015890-G-T

100962269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9015487-T-C

100962269-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9015487-T-G

http://identifiers.org/hco/11/GRCh38#100962325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9015439-C-A

100962325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9015439-C-T

100962350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9015414-G-A

100962350-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9015414-G-T

100962354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9015410-A-G

http://identifiers.org/hco/11/GRCh38#100962474-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9015292-A-C

100962474-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 9015292-A-T

100963155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9013928-A-G

100963174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9013907-A-G

100963202-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9013881-C-G

100963202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9013881-C-T

http://identifiers.org/hco/11/GRCh38#100963324-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9013753-A-C

100963324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9013753-A-G

100963460-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9013591-A-T

100963560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9013468-G-A

100963569-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9013459-A-T

100963705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9013324-C-T

100963720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9013312-A-G

100963791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9013249-A-G

100964182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9012924-A-G

100964244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9012882-G-A

100964262-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9012864-T-C

100964262-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9012864-T-G

100964301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9012840-A-G

100964523-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9012684-A-T

100964626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9012602-A-G

100964715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9012544-A-G

100964759-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9012501-C-G

100965240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9012052-G-A

100965253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9012033-A-G

http://identifiers.org/hco/11/GRCh38#100965365-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9011904-A-C

100965424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9011844-G-A

100965478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9011801-T-C

100965494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9011785-A-G

http://identifiers.org/hco/11/GRCh38#100965533-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9011747-A-C

100965533-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9011747-A-T

http://identifiers.org/hco/11/GRCh38#100965570-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9011711-A-C

100965570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9011711-A-G

100965608-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9011673-T-A

100965608-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9011673-T-G

100965612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9011570-T-C

http://identifiers.org/hco/11/GRCh38#100965619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9011520-C-A

100965619-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9011520-C-G

100965619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9011520-C-T

100965676-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 9011435-G-T

100965700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 9011411-G-A

100965700-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 9011411-G-T

100965808-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9011303-T-A

100965808-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9011303-T-G

100965856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9011256-A-G

100965931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9011181-T-C

100965955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9011157-T-C

100966089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9011030-G-A

100966165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9010943-C-T

http://identifiers.org/hco/11/GRCh38#100973096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9009511-C-A

100973096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9009511-C-T

100973311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 9009299-A-G

100973453-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9009140-G-C

100973453-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9009140-G-T

http://identifiers.org/hco/11/GRCh38#100973463-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9009130-C-A

100973530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9009072-C-T

100973665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9008940-T-C

100973728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9008766-A-G

100973786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9008707-A-G

100973786-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9008707-A-T

100973891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9008629-G-A

100974064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9008491-C-T

100974124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9008433-A-G

100974253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9008315-C-T

http://identifiers.org/hco/11/GRCh38#100974317-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9008258-C-A

100974350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9008223-T-C

100974411-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9008158-G-T

100974474-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 9008096-C-G

100974626-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9007945-A-T

100974653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9007918-A-G

100974676-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9007895-T-G

100974698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9007876-T-C

100974710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9007864-T-C

100974818-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9007755-G-T

100974894-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9007680-C-G

100974894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9007680-C-T

100974948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9007628-C-T

http://identifiers.org/hco/11/GRCh38#100975027-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9007538-A-C

100975141-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9007423-A-T

100975727-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9006976-C-G

100975781-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9006922-G-T

100975873-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9006823-T-G

100975917-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9006778-T-G

http://identifiers.org/hco/11/GRCh38#100975965-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9006730-A-C

100975965-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9006730-A-T

100975989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9006707-G-A

100975989-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9006707-G-T

100976568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9006136-G-T

100976681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9006019-G-A

100976681-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9006019-G-T

100976719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9005985-A-G

100976719-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9005985-A-T

100976856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 9005848-G-A

100976980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9005722-G-A

http://identifiers.org/hco/11/GRCh38#100977021-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9005681-A-C

100977025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9005677-G-A

100977025-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9005677-G-C

100977025-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9005677-G-T

http://identifiers.org/hco/11/GRCh38#100977033-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9005669-C-A

100977033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9005669-C-T

100977082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9005634-A-G

100977082-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9005634-A-T

100977114-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9005608-G-C

100977114-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9005608-G-T

100977522-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9005278-G-C

100977586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9005214-G-A

http://identifiers.org/hco/11/GRCh38#100977595-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9005207-A-C

100977668-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9005136-C-G

100977693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9005111-T-C

100977754-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9005044-A-T

100977836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9004974-C-T

100977852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9004958-G-A

100978004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9004809-C-T

100978121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9004719-A-G

100978222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9004609-G-A

100978249-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9004576-T-A

100978350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9004363-T-C

100978585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9004113-T-C

100978686-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9004016-G-C

100978688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9004014-G-A

http://identifiers.org/hco/11/GRCh38#100978820-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9003893-A-C

100978820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9003893-A-G

100978840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9003875-A-G

100978873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9003842-G-A

100978873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9003842-G-T

100978883-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9003832-C-G

100978896-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9003821-T-G

100978901-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9003816-T-G

http://identifiers.org/hco/11/GRCh38#100978934-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9003783-C-A

http://identifiers.org/hco/11/GRCh38#100978967-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9003701-C-A

100978967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9003701-C-T

100978997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 9003671-A-G

100979034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 9003634-C-T

100979039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 9003629-T-C

100979054-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9003614-G-C

100979072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9003595-T-C

100979088-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9003565-T-G

100979109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9003545-T-C

http://identifiers.org/hco/11/GRCh38#100979130-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9003524-C-A

100979295-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9003139-A-T

100979328-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9003102-A-T

100979406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9003027-A-G

100979421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9003014-G-A

100979512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9002953-G-A

100980979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9000801-T-C

http://identifiers.org/hco/11/GRCh38#100981414-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#9000375-C-A

100981643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 9000182-T-C

100982202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8999761-C-T

http://identifiers.org/hco/11/GRCh38#100986767-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#8999472-C-A

100986864-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8999381-A-T

http://identifiers.org/hco/11/GRCh38#100987139-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#8999135-A-C

100987478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8998276-T-C

100987480-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8998274-T-A

100987480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8998274-T-C

100987617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8998138-T-C

100988631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8997783-A-G

100988631-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 8997783-A-T

100988717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 8997680-C-T

http://identifiers.org/hco/11/GRCh38#100988911-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#8997488-A-C

100989072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: 8997333-T-C

100989072-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: 8997333-T-G

100989437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: 8996966-T-C

100989453-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: 8996950-G-T

100989539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: 8996845-T-C

100989546-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: 8996838-T-A

100990049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: 8996138-C-T

100990134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: 8996051-T-C

100990249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: 8995957-A-G

http://identifiers.org/hco/11/GRCh38#100990273-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#8995933-C-A

100990306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: 8995906-T-C

100990320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: 8995895-A-G

100990324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: 8995891-G-A

100990330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: 8995885-T-C

http://identifiers.org/hco/11/GRCh38#100990343-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#8995872-C-A

100990349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: 8995866-A-G

http://identifiers.org/hco/11/GRCh38#100990386-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#8995829-C-A

http://identifiers.org/hco/11/GRCh38#100990514-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#8995707-A-C

100990514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: 8995707-A-G

http://identifiers.org/hco/11/GRCh38#100990611-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#8995614-C-A

100990614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: 8995611-T-C

http://identifiers.org/hco/11/GRCh38#100990638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#8995590-C-A

100990667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: 8995560-G-T

100990726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: 8995496-A-G

100990726-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: 8995496-A-T

100990736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: 8995486-T-C

100990765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: 8995460-A-G

http://identifiers.org/hco/11/GRCh38#100990783-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#8995454-C-A

100990830-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: 8995408-T-G

100990896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: 8995346-T-C

100990922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: 8995319-G-A

100990922-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: 8995319-G-T

http://identifiers.org/hco/11/GRCh38#100990939-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#8995302-C-A

100990944-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: 8995297-G-T

100991129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: 8995131-T-C

100991130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: 8995130-T-C

100991131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: 8995129-G-A

100991131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: 8995129-G-T

http://identifiers.org/hco/11/GRCh38#100991139-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#8995122-A-C

100991184-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: 8995092-T-A

100991293-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: 8994982-A-T

100991307-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: 8994968-T-G

http://identifiers.org/hco/11/GRCh38#100991326-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#8994949-C-A

100991339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: 8994936-T-C

100991387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: 8994893-T-C

100991584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: 8994714-G-A

100991679-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: 8994611-G-T

100991686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: 8994604-C-T

100991704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: 8994586-A-G

100991804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: 8994483-T-C

100991927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: 8994339-T-C

100991927-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: 8994339-T-G

100991968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: 8994297-A-G

http://identifiers.org/hco/11/GRCh38#100991993-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#8994247-C-A

100992034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: 8994210-T-C

100992152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant
orthologous variants: 8993893-T-C

100992183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant
orthologous variants: 8993839-A-G

100992220-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant
orthologous variants: 8993775-T-A

100992220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant
orthologous variants: 8993775-T-C

100992244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant
orthologous variants: 8993743-A-G

100992281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant
orthologous variants: 8993707-G-A

100992281-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant
orthologous variants: 8993707-G-C

100992324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 8993664-T-C

100992375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 8993620-A-G

100992389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 8993606-T-C

100992410-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 8993585-G-C

100992419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 8993576-T-C

100992458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 8993548-C-T

100992467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 8993539-T-C

100992642-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 8993372-C-G

100992689-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 8993344-T-G

http://identifiers.org/hco/11/GRCh38#100992719-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#8993322-A-C

100992721-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: 8993320-T-A

http://identifiers.org/hco/11/GRCh38#100992727-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#8993314-A-C

100992727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: 8993314-A-G

100992765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: 8993274-T-C

100992765-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: 8993274-T-G

100992789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: 8993255-A-G

100992789-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: 8993255-A-T

http://identifiers.org/hco/11/GRCh38#100992850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#8993197-C-A

100992850-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: 8993197-C-G

100992858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: 8993188-A-G

100992858-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: 8993188-A-T

100992860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: 8993186-A-G

100992879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: 8993167-G-A

100992879-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: 8993167-G-C

100992879-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: 8993167-G-T

http://identifiers.org/hco/11/GRCh38#100992884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#8993160-C-A

100992884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: 8993160-C-T

100992916-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: 8993131-T-A

100992916-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: 8993131-T-G

100992917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: 8993130-G-A

100992917-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: 8993130-G-T

100992965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: 8993082-A-G

http://identifiers.org/hco/11/GRCh38#100993001-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#8993046-A-C

100993001-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: 8993046-A-T

http://identifiers.org/hco/11/GRCh38#100993032-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#8993040-A-C

100993032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: 8993040-A-G

http://identifiers.org/hco/11/GRCh38#100993033-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#8993039-A-C

100993089-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: 8992983-T-A

100993102-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: 8992970-G-T

100993188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: 8992893-G-A

100993188-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: 8992893-G-T

http://identifiers.org/hco/11/GRCh38#100993433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#8992750-C-A

100993440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: 8992743-G-A

100993440-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: 8992743-G-T

100993457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: 8992726-A-G

100993862-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26545
most severe consequence: 3 prime UTR variant
orthologous variants: 8992433-A-T