114239278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 5 prime UTR variant
orthologous variants: 56862511-G-A

114239278-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 5 prime UTR variant
orthologous variants: 56862511-G-C

114239278-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 5 prime UTR variant
orthologous variants: 56862511-G-T

http://identifiers.org/hco/10/GRCh38#114239283-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56862516-C-A

114239312-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 5 prime UTR variant
orthologous variants: 56862536-T-G

114239329-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 5 prime UTR variant
orthologous variants: 56862554-G-T

http://identifiers.org/hco/10/GRCh38#114239332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56862557-C-A

114239332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56862557-C-T

114239334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56862567-G-A

114239334-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56862567-G-C

114239334-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56862567-G-T

114239382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56862619-A-G

114239406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56862672-G-A

114239452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 56862717-G-A

114239452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 56862717-G-T

114239498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 56862739-T-C

114239590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56862825-G-T

114239656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56862875-G-A

114239656-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56862875-G-C

114239656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56862875-G-T

114239660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56862883-C-T

http://identifiers.org/hco/10/GRCh38#114239672-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56862893-C-A

114239701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56862908-G-A

114239701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56862908-G-T

http://identifiers.org/hco/10/GRCh38#114239706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56862913-C-A

114239706-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56862913-C-G

114239706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56862913-C-T

114239738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56862946-G-T

114239827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 56863004-G-A

114239827-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 56863004-G-T

114239867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56863041-A-G

114240179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56863288-G-A

114240193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56863302-T-C

114240232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56863339-T-C

114240258-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56863350-A-T

114240324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56863426-G-A

114240327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56863429-G-A

114240639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56863708-G-A

114240902-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56863832-T-A

114240911-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56863846-G-C

114240911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56863846-G-T

114241254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56864154-G-A

114241426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56864262-T-C

114241426-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56864262-T-G

114241497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56864330-T-C

114241623-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56864457-T-C

114241814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56864672-G-A

114241814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56864672-G-T

114241819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56864677-C-T

114242030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56865190-T-C

http://identifiers.org/hco/10/GRCh38#114242180-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56865328-A-C

114242664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56865574-G-A

114242672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56865582-C-T

114242756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56865653-A-G

http://identifiers.org/hco/10/GRCh38#114242820-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56865707-A-C

114242837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56865721-T-C

114242880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56865764-C-T

114242935-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56865798-A-T

114243119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56865990-A-G

114243331-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56866165-G-C

114243488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56866511-C-T

114243489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56866512-G-A

114243633-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56866654-A-G

114243690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56866704-C-T

114244139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56867068-T-C

114244316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56867231-C-T

114244524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56867354-A-G

114244524-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56867354-A-T

114245289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56868314-G-A

http://identifiers.org/hco/10/GRCh38#114245709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56868705-C-A

114248442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56869317-G-A

http://identifiers.org/hco/10/GRCh38#114248571-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56869434-A-C

114248571-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56869434-A-T

http://identifiers.org/hco/10/GRCh38#114248588-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56869459-C-A

http://identifiers.org/hco/10/GRCh38#114248594-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56869465-C-A

114248594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56869465-C-T

114248630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56869481-T-C

114248649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56869499-G-A

114248649-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56869499-G-C

114248649-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56869499-G-T

114248676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56869526-C-T

114248695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56869548-T-C

114249835-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56870235-T-G

http://identifiers.org/hco/10/GRCh38#114249883-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56870287-C-A

114249883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56870287-C-T

114249976-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56870360-A-T

114250103-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56870483-C-G

114250196-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56870560-T-G

114250288-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56870637-C-G

114250344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56870689-C-T

114250505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56870821-G-A

http://identifiers.org/hco/10/GRCh38#114250521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56870840-C-A

114250628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56870929-C-T

114250795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56871032-C-T

114250895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56871119-T-C

114251137-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56871310-A-T

114251170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56871343-A-G

114251182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56871363-G-A

114251263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56871433-C-T

114251272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56871441-G-A

114251427-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56871584-G-C

114251506-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56871650-G-C

114251510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56871654-G-A

114251660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56871797-C-T

114251769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56871892-C-T

http://identifiers.org/hco/10/GRCh38#114253553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56873359-C-A

114253553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56873359-C-T

http://identifiers.org/hco/10/GRCh38#114253579-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56873384-C-A

http://identifiers.org/hco/10/GRCh38#114253748-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56873549-C-A

114253748-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56873549-C-G

114253754-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56873555-G-C

http://identifiers.org/hco/10/GRCh38#114254907-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56875304-C-A

114254936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 56875331-T-C

114254937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 56875332-G-A

114255091-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56875477-G-T

114255132-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56875518-C-G

114255155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56875541-G-A

114255155-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56875541-G-T

114255278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56875686-C-T

114255303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56875709-C-T

114255353-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56875767-T-A

114255364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56875784-C-T

114255616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56876091-G-A

114255623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56876096-A-G

114257359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56877532-A-G

114257428-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56877616-C-G

114257698-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56878452-A-T

114258039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56879429-A-G

114258084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56879473-T-C

114258162-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56879510-T-G

http://identifiers.org/hco/10/GRCh38#114258237-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56879557-C-A

114258237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56879557-C-T

114258344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56879648-T-C

114258364-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56879666-T-A

114258457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56879741-C-T

114258725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56880015-G-A

114258726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56880016-C-T

114258738-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56880063-A-T

114258894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56880344-G-A

114258894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56880344-G-T

114258976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56880424-T-C

114258981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56880429-G-A

114259114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56880543-A-G

114259119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56880548-C-T

114259424-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56880796-G-C

114259449-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56880821-G-T

114259526-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56880888-A-T

114259773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56881090-C-T

114259899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56881203-A-G

114259955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56881231-G-A

114260180-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56881364-G-C

114260201-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56881378-A-T

114260389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56881503-A-G

114260456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56881565-T-C

114260741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56881776-A-G

114261081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56882105-A-G

114261082-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56882106-G-C

114261082-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56882106-G-T

114261096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56882118-G-A

114261096-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56882118-G-T

114261097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56882119-G-A

114261097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56882119-G-T

114261131-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 56882139-A-T

114261157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 56882172-G-A

114261223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 56882235-A-G

114261282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 56882294-A-G

114261430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56882782-T-C

114261446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56882787-C-T

114261485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56882824-C-T

114272595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56886168-G-A

114272595-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56886168-G-T

114272627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56886200-G-T

114272634-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56886206-A-G

http://identifiers.org/hco/10/GRCh38#114272695-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56886265-C-A

114272752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 56886318-G-A

114272758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 56886324-G-A

114272758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 56886324-G-T

http://identifiers.org/hco/10/GRCh38#114272776-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: http://identifiers.org/mco/19/GRCm39#56886342-C-A

114272776-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 56886342-C-G

114272776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 56886342-C-T

114272837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 56886400-G-A

114272837-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 56886400-G-C

114272842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 56886405-T-C

114272842-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 56886405-T-G

114272915-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 56886478-G-C

http://identifiers.org/hco/10/GRCh38#114272949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56886516-C-A

114272949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56886516-C-T

http://identifiers.org/hco/10/GRCh38#114272986-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56886552-C-A

114272986-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56886552-C-G

114272986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56886552-C-T

114273001-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56886569-G-T

http://identifiers.org/hco/10/GRCh38#114273028-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56886601-C-A

114273028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56886601-C-T

http://identifiers.org/hco/10/GRCh38#114273049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56886629-C-A

114273049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56886629-C-T

114273050-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56886630-T-C

http://identifiers.org/hco/10/GRCh38#114273059-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56886640-C-A

114273059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56886640-C-T

114273182-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56886763-T-G

114273291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56886881-A-G

114273320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56886901-T-C

114273321-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56886902-C-G

114273333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56886914-C-T

114273361-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56886942-T-G

http://identifiers.org/hco/10/GRCh38#114273588-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56887149-A-C

http://identifiers.org/hco/10/GRCh38#114278024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56890070-C-A

114278024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 56890070-C-T

114278213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56890249-C-T

http://identifiers.org/hco/10/GRCh38#114278594-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56890547-A-C

114278594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56890547-A-G

114278598-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56890551-G-T

http://identifiers.org/hco/10/GRCh38#114278599-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56890552-C-A

114278599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56890552-C-T

114278606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56890559-G-A

114278606-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56890559-G-T

114278622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56890574-C-T

http://identifiers.org/hco/10/GRCh38#114278638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56890584-C-A

114278638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56890584-C-T

http://identifiers.org/hco/10/GRCh38#114278678-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56890619-C-A

114278678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56890619-C-T

114278706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56890648-G-A

114278709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56890652-G-A

114278832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 56890781-G-A

http://identifiers.org/hco/10/GRCh38#114278858-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56890807-C-A

114278865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56890814-G-A

114278865-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56890814-G-C

114278880-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56890820-G-C

114278880-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56890820-G-T

114278911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56890856-G-T

http://identifiers.org/hco/10/GRCh38#114281300-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56890974-C-A

114281403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56891049-G-A

114281403-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56891049-G-T

114281631-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 56891194-G-T

114281657-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 56891227-A-T

114281658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 56891228-C-T

114281752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 56891308-C-T

114281799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56891353-G-A

114281799-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56891353-G-C

114281799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56891353-G-T

114281807-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56891360-T-G

114281859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56891409-G-A

114281859-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56891409-G-T

114281920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56891475-C-T

114282046-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56891580-G-T

114282058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56891597-G-A

114282066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56891609-G-A

114282071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56891614-G-A

114282093-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56891638-T-A

114282369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56891814-G-A

114282369-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56891814-G-T

http://identifiers.org/hco/10/GRCh38#114282626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56891997-C-A

114282626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56891997-C-T

http://identifiers.org/hco/10/GRCh38#114282645-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56892016-C-A

114282645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56892016-C-T

http://identifiers.org/hco/10/GRCh38#114282649-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56892020-C-A

114282649-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56892020-C-G

114282649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56892020-C-T

114282675-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56892044-T-A

114282679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56892048-T-C

114282714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56892079-G-A

http://identifiers.org/hco/10/GRCh38#114282848-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56892213-C-A

http://identifiers.org/hco/10/GRCh38#114283064-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56892386-C-A

114283064-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56892386-C-G

114283064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56892386-C-T

114283696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56892781-A-G

114283753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56892835-C-T

114283895-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56892950-C-G

114284088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56893138-A-G

http://identifiers.org/hco/10/GRCh38#114284108-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56893153-A-C

114284146-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56893195-G-T

114284183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56893230-T-C

114284212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56893259-C-T

114284243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56893290-A-G

114284286-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56893331-C-G

114284294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56893339-G-A

114284294-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56893339-G-T

114284397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56893410-C-T

114284446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56893459-G-A

114284632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56893638-G-A

114284738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56893822-T-C

114284769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56893839-A-G

114284769-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56893839-A-T

114284772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56893842-G-A

114284772-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56893842-G-T

114284915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 56893963-A-G

114285016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56894063-A-G

114285067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56894122-A-G

http://identifiers.org/hco/10/GRCh38#114285092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56894147-C-A

114285092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56894147-C-T

http://identifiers.org/hco/10/GRCh38#114285124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56894176-C-A

114285124-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56894176-C-G

114285124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56894176-C-T

114285180-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56894204-A-T

114285352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56894321-G-A

114285386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56894354-A-G

114285390-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56894358-G-C

114285417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56894371-T-C

114285437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56894391-G-A

114285484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56894427-T-C

114285820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56894683-G-A

114285820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56894683-G-T

114285855-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56894717-G-C

114285855-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56894717-G-T

http://identifiers.org/hco/10/GRCh38#114285868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56894750-C-A

114285868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56894750-C-T

114286007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 56894890-C-T

114286036-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 56894919-C-G

114286036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 56894919-C-T

114286037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 56894920-G-A

114286037-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 56894920-G-C

114286037-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 56894920-G-T

http://identifiers.org/hco/10/GRCh38#114286084-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56894967-A-C

114286087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 56894970-G-A

114286123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 56895006-G-A

114286288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 56895171-G-A

114286307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 56895190-C-T

114286338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 56895221-G-A

114286338-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 56895221-G-T

114286361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 56895244-C-T

114286388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 56895271-G-A

114286474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 56895357-T-C

114286522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56895405-A-G

114286526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56895409-C-T

114286527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56895410-C-T

http://identifiers.org/hco/10/GRCh38#114286533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56895416-C-A

http://identifiers.org/hco/10/GRCh38#114286574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56895462-C-A

114286574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56895462-C-T

114286593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56895480-T-C

114286618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56895504-G-A

114286618-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56895504-G-T

114286760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56895586-A-G

114287000-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56895745-C-G

http://identifiers.org/hco/10/GRCh38#114287923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56896273-C-A

114288037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56896392-C-T

114288084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56896438-C-T

http://identifiers.org/hco/10/GRCh38#114288087-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56896441-A-C

114288208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56896558-G-A

114288427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56896771-G-A

114288442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56896784-T-C

114288656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56896979-A-G

114288668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56897002-T-C

114288686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56897026-T-C

114288700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56897040-G-A

114288849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56897188-G-A

114288849-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56897188-G-T

114288860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56897199-A-G

http://identifiers.org/hco/10/GRCh38#114288866-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56897207-C-A

114288866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56897207-C-T

114288892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56897217-C-T

114288990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 56897316-A-G

114289041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 56897367-C-T

114289116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 56897442-C-T

114289135-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 56897461-A-T

114289290-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 56897616-C-G

114289290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 56897616-C-T

114289351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 56897677-G-A

114289374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 56897700-T-C

114289413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 56897739-G-A

114289413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 56897739-G-T

http://identifiers.org/hco/10/GRCh38#114289443-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56897769-C-A

114289443-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 56897769-C-G

114289443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 56897769-C-T

http://identifiers.org/hco/10/GRCh38#114289510-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56897836-C-A

114289510-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 56897836-C-G

114289510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 56897836-C-T

114289525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 56897853-C-T

114289541-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 56897869-C-G

114289585-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56897910-A-T

114290174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 56898072-G-A

114290205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 56898102-G-A

114290205-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 56898102-G-C

114290205-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 56898102-G-T

114290207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 56898104-C-T

http://identifiers.org/hco/10/GRCh38#114290231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56898113-C-A

114290246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, missense_variant
orthologous variants: 56898128-A-G

114290310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 56898192-T-C

114290399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron variant
orthologous variants: 56898279-A-G

114290420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron variant
orthologous variants: 56898300-G-A

http://identifiers.org/hco/10/GRCh38#114290427-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56898307-C-A

114290427-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron variant
orthologous variants: 56898307-C-G

114290427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron variant
orthologous variants: 56898307-C-T

http://identifiers.org/hco/10/GRCh38#114290459-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56898337-C-A

114290459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron variant
orthologous variants: 56898337-C-T

114290505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron variant
orthologous variants: 56898370-T-C

114290559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron variant
orthologous variants: 56898442-G-T

114290572-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron variant
orthologous variants: 56898455-T-G

114290606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron variant
orthologous variants: 56898486-T-C

http://identifiers.org/hco/10/GRCh38#114290634-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56898540-C-A

114290659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron variant
orthologous variants: 56898584-T-C

114290787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron variant
orthologous variants: 56898723-C-T

114290796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron variant
orthologous variants: 56898732-G-A

114290844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron variant
orthologous variants: 56898772-A-G

114291000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron variant
orthologous variants: 56898863-G-A

http://identifiers.org/hco/10/GRCh38#114291091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56898950-C-A

http://identifiers.org/hco/10/GRCh38#114291243-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56899077-A-C

114291243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 56899077-A-G

114291243-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 56899077-A-T

114291266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 56899109-C-T

http://identifiers.org/hco/10/GRCh38#114291270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56899113-C-A

114291270-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 56899113-C-G

114291270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 56899113-C-T

114291343-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 56899185-C-G

114291343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 56899185-C-T

http://identifiers.org/hco/10/GRCh38#114291369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56899211-C-A

114291369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 56899211-C-T

http://identifiers.org/hco/10/GRCh38#114291422-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56899224-C-A

114291456-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 56899252-A-T

114291489-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 56899280-T-A

114291489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 56899280-T-C

114291516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 56899303-T-C

http://identifiers.org/hco/10/GRCh38#114291550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56899337-C-A

114291550-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 56899337-C-G

http://identifiers.org/hco/10/GRCh38#114291647-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56899421-C-A

114291647-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 56899421-C-G

114291647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 56899421-C-T

114291654-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 56899428-G-T

114291787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 56899537-A-G

114291879-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 56899631-T-G

114291896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 56899644-G-A

114291959-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 56899688-T-G

114294292-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 56900338-G-T

114294313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 56900359-T-C

114294427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24709
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 56900442-G-A