http://identifiers.org/hco/11/GRCh38#107591103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53882604-C-A

107591103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: 5 prime UTR variant
orthologous variants: 53882604-C-T

107591228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 53882479-G-A

107591228-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 53882479-G-C

107591228-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 53882479-G-T

107591372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 53882344-C-T

http://identifiers.org/hco/11/GRCh38#107591393-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#53882323-C-A

107591393-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 53882323-C-G

107591404-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 53882312-G-T

http://identifiers.org/hco/11/GRCh38#107591422-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53882294-C-A

107591675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53882080-G-A

107591737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53882017-G-A

107591737-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53882017-G-T

http://identifiers.org/hco/11/GRCh38#107592019-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53881770-A-C

http://identifiers.org/hco/11/GRCh38#107592142-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53881666-C-A

http://identifiers.org/hco/11/GRCh38#107592144-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53881664-C-A

107592144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53881664-C-T

107592266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53881539-G-T

http://identifiers.org/hco/11/GRCh38#107592267-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53881538-C-A

107592267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53881538-C-T

http://identifiers.org/hco/11/GRCh38#107592274-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53881531-C-A

107592274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53881531-C-T

http://identifiers.org/hco/11/GRCh38#107592291-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53881493-C-A

107592291-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53881493-C-G

107592644-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53881136-G-C

107592645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53881135-T-C

107592746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53881034-G-A

107592746-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53881034-G-C

107592783-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53881000-G-C

107592783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53881000-G-T

http://identifiers.org/hco/11/GRCh38#107593052-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53880736-A-C

107593070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53880718-A-G

107593160-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53880624-G-C

107593246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53880541-T-C

107593480-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53880355-C-G

107593514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53880321-G-A

107593795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53880040-G-A

107594064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53879780-G-A

107594145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53879675-G-A

107594162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53879658-A-G

107594265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53879547-G-A

107594537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53879167-T-C

107595009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53878445-G-A

107595102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53878352-A-G

107595426-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53877827-T-A

107595731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53877537-A-G

107596337-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53876318-T-A

107596431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53876215-A-G

107597015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53874374-A-G

107597155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53874277-T-C

107597494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53873967-G-A

107597682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53873783-A-G

107597901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53873569-G-A

107597902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53873568-G-A

107598502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53872916-G-A

107598605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53872815-A-G

107599184-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53865911-G-C

http://identifiers.org/hco/11/GRCh38#107606007-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53864168-C-A

107606167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53864010-A-G

107609186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53862770-G-A

107609281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53862616-T-C

107609445-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53862455-T-A

107609915-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53861992-G-C

107612880-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53860881-T-G

107612948-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53860819-T-A

http://identifiers.org/hco/11/GRCh38#107613028-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53860741-A-C

107613273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53860511-A-G

107613438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53860356-A-G

107613713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53860076-T-C

107618045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53854274-T-C

107618045-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53854274-T-G

107618167-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 53854170-T-A

107618184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 53854152-G-A

107618184-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 53854152-G-T

107618213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 53854123-G-A

107618213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 53854123-G-T

http://identifiers.org/hco/11/GRCh38#107618350-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53854002-A-C

107618350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53854002-A-G

107618353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53853999-A-G

107618353-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53853999-A-T

http://identifiers.org/hco/11/GRCh38#107618355-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53853997-C-A

107618355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53853997-C-T

107618389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53853962-C-T

107618472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53853880-A-G

107618474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53853878-G-A

107619146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53853275-T-C

107619310-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53853129-T-G

107619680-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53852826-T-G

107619820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53852697-C-T

107620044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53852092-C-T

107620358-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53851753-G-T

107620421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53851690-A-G

107620432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53851677-A-G

http://identifiers.org/hco/11/GRCh38#107620456-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53851653-A-C

107620456-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53851653-A-T

107620503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53851598-A-G

107620923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53851499-A-G

107621058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53851363-T-C

107621119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53851299-T-C

107621119-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53851299-T-G

107621222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53851198-C-T

107621361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53851061-A-G

107621387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53851039-G-A

107621387-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53851039-G-T

107621473-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53850959-G-T

107621583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53850890-G-A

107621583-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53850890-G-T

http://identifiers.org/hco/11/GRCh38#107621721-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53850795-A-C

107621721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53850795-A-G

107621721-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53850795-A-T

107622238-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53850525-G-T

107622424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53850349-T-C

107622584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53850215-C-T

107622649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53850150-A-G

http://identifiers.org/hco/11/GRCh38#107622888-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53849885-A-C

107622888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53849885-A-G

107622944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53849828-A-G

http://identifiers.org/hco/11/GRCh38#107623047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53849769-C-A

107623204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53849750-T-C

http://identifiers.org/hco/11/GRCh38#107623240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53849718-C-A

107623406-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 53849638-G-T

107623448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 53849594-G-A

107623448-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 53849594-G-T

107623500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 53849547-T-C

http://identifiers.org/hco/11/GRCh38#107623583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53849468-C-A

107624708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53848502-T-C

107624981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53848236-G-A

107625116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53848109-C-T

107625148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53848077-T-C

107625183-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53848043-T-G

107625241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53847985-A-G

107625282-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53847953-T-A

107625282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53847953-T-C

107625297-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53847938-G-T

http://identifiers.org/hco/11/GRCh38#107625301-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53847934-A-C

107625533-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, splice_donor_variant
orthologous variants: 53847679-G-T

107625543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53847669-C-T

http://identifiers.org/hco/11/GRCh38#107625611-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53847609-C-A

107625611-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53847609-C-G

107625636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53847585-G-A

107625636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53847585-G-T

107625679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53847543-A-G

107625856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53847383-A-G

107625987-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53847273-A-T

http://identifiers.org/hco/11/GRCh38#107626327-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53847072-C-A

107626439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53846994-T-C

107626439-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53846994-T-G

107626510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53846930-C-T

107626660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53846870-C-T

107626679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53846853-A-G

http://identifiers.org/hco/11/GRCh38#107626757-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53846787-C-A

http://identifiers.org/hco/11/GRCh38#107626851-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53846697-A-C

107627167-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53846280-T-A

http://identifiers.org/hco/11/GRCh38#107627253-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53846111-C-A

107627253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53846111-C-T

http://identifiers.org/hco/11/GRCh38#107627280-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53846084-C-A

107627574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53845778-G-A

107627788-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53845297-A-T

107628077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53844901-T-C

http://identifiers.org/hco/11/GRCh38#107628133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53844849-C-A

107628525-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53844771-G-T

107628770-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53844579-T-A

107628827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53844530-A-G

107629042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53844364-A-G

107629067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53844339-T-C

107629240-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53844136-T-G

107629385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53844003-A-G

107629515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53843908-C-T

107629822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53843673-A-G

107629903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53843610-G-A

107630025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53843492-G-A

107630025-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53843492-G-C

107630054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53843454-C-T

107630366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53843208-T-C

http://identifiers.org/hco/11/GRCh38#107630487-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53843087-A-C

107630523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: missense variant
orthologous variants: 53843051-T-C

http://identifiers.org/hco/11/GRCh38#107630688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53842883-C-A

107630688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53842883-C-T

http://identifiers.org/hco/11/GRCh38#107630747-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53842824-C-A

107630747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53842824-C-T

107630767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53842805-G-A

107630767-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53842805-G-C

107630926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53842529-G-A

107631264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53841878-T-C

107631420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53841648-G-A

107631420-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53841648-G-C

http://identifiers.org/hco/11/GRCh38#107631452-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53841616-C-A

107631452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53841616-C-T

107631616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: missense variant
orthologous variants: 53841460-A-G

107631715-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53841361-A-T

107631720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53841356-A-G

107631728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53841348-A-G

107631728-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53841348-A-T

107632246-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53840661-A-T

107632422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53840484-T-C

107635532-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53838969-T-G

107635538-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53838963-A-T

107635605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53838889-T-C

107635619-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53838875-G-C

107635869-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53838666-G-T

http://identifiers.org/hco/11/GRCh38#107635878-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53838657-A-C

107635880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53838655-G-A

107635880-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53838655-G-T

http://identifiers.org/hco/11/GRCh38#107635914-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53838620-C-A

107635914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53838620-C-T

107636007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53838529-G-A

107636007-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53838529-G-T

107636791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53837590-C-T

107637044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53837342-A-G

http://identifiers.org/hco/11/GRCh38#107638106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53835918-C-A

107638106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53835918-C-T

107638136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53835890-T-C

107646234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53834113-C-T

107646879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53833823-T-C

107646907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53833796-G-A

107646925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53833767-G-A

107647119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53833645-A-G

107647160-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53833609-A-T

107647182-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53833584-G-C

107647454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53833395-T-C

107647454-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53833395-T-G

107647508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: missense variant
orthologous variants: 53833341-G-A

107647508-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: missense variant
orthologous variants: 53833341-G-T

107647620-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53833229-A-T

107647622-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53833227-C-G

107647622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53833227-C-T

http://identifiers.org/hco/11/GRCh38#107647722-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53833137-C-A

107647722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53833137-C-T

107647779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53833076-T-C

107647824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53833024-T-C

http://identifiers.org/hco/11/GRCh38#107647860-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53832995-A-C

107647860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53832995-A-G

107647986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53832884-A-G

107649727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53832603-A-G

107649965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53832010-A-G

107649971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53832001-C-T

107650075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53831906-G-A

107650208-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53831869-G-T

http://identifiers.org/hco/11/GRCh38#107650222-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53831855-C-A

107650222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53831855-C-T

http://identifiers.org/hco/11/GRCh38#107650240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53831837-C-A

107650271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53831806-A-G

107650271-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53831806-A-T

107650287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53831790-G-A

107650287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53831790-G-T

http://identifiers.org/hco/11/GRCh38#107650387-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53831698-C-A

107650387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: missense variant
orthologous variants: 53831698-C-T

107650418-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53831667-T-A

107650504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53831583-G-A

107650504-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53831583-G-C

107650504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53831583-G-T

http://identifiers.org/hco/11/GRCh38#107650512-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53831575-C-A

107650512-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53831575-C-G

107650512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53831575-C-T

http://identifiers.org/hco/11/GRCh38#107650541-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53831544-C-A

107650770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53831343-G-A

107650770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53831343-G-T

107650834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53831299-T-C

107650844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53831289-T-C

107650941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53831195-T-C

107651057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53831081-G-A

107651057-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53831081-G-C

107651057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53831081-G-T

107651097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53831040-C-T

107651133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53831017-C-T

107651139-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53831011-C-G

107651139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53831011-C-T

http://identifiers.org/hco/11/GRCh38#107651202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53830949-C-A

107651234-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53830926-G-C

107651831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53830173-G-A

http://identifiers.org/hco/11/GRCh38#107651968-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53830043-A-C

107652125-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53829913-G-T

107652742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53829340-T-C

http://identifiers.org/hco/11/GRCh38#107653012-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53829445-A-C

107653137-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53829580-T-A

107653137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53829580-T-C

107654058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 53828767-T-C

http://identifiers.org/hco/11/GRCh38#107654203-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53828624-A-C

107654203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53828624-A-G

107655057-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53827916-T-C

http://identifiers.org/hco/11/GRCh38#107655889-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53827053-C-A

107656074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 53826868-T-C

107656104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53826838-T-C

107656602-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53826754-T-G

107656629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53826724-A-G

107656753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53826611-T-C

107656810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53826554-A-G

107656932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53826419-A-G

107657070-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53826211-G-C

107657921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53825659-C-T

107657995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53825581-A-G

http://identifiers.org/hco/11/GRCh38#107658000-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53825577-A-C

107658031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53825547-G-A

107658050-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53825533-T-C

107658205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53825403-G-A

107658492-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53825136-G-T

107658590-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53825094-A-T

107659648-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53824267-T-G

107659651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53824264-G-A

107659654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53824261-G-A

107659672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53824243-T-C

107660065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53823998-C-T

107660143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53823920-T-C

107660199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53823860-C-T

107660248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53823809-T-C

107660248-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53823809-T-G

107660372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53823689-G-A

107660555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53823511-C-T

107660557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53823509-A-G

107660647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53823424-C-T

107660825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53823246-A-G

107660856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53823215-T-C

107660949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53823118-A-G

107661029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53823039-G-A

107661200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53822863-G-A

107661246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53822844-C-T

107661364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53822728-C-T

107661744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53821677-C-T

107664641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53821291-G-A

107664641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53821291-G-T

107664737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53820429-A-G

107664874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53820294-A-G

107664874-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53820294-A-T

107664932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53820255-G-A

107664932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53820255-G-T

107664964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: intron variant
orthologous variants: 53820233-T-C

107665093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: missense variant
orthologous variants: 53820108-C-T

107665150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: missense variant
orthologous variants: 53820051-G-A

107665159-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: missense variant
orthologous variants: 53820042-C-G

107665448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: 3 prime UTR variant
orthologous variants: 53819713-G-A

107665448-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: 3 prime UTR variant
orthologous variants: 53819713-G-T

107665501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: 3 prime UTR variant
orthologous variants: 53819659-T-C

107665533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: 3 prime UTR variant
orthologous variants: 53819624-T-C

107666337-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25334
most severe consequence: 3 prime UTR variant
orthologous variants: 53819168-G-C