91409294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36531174-T-C

91409302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36531183-T-C

91409486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36531355-T-C

91409723-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36531598-T-G

91410091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36531827-G-A

91410127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36531874-T-C

91410127-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36531874-T-G

91410159-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36531903-T-G

91410180-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36531927-C-G

91410180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36531927-C-T

91410193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36531940-G-A

91410193-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36531940-G-C

91410226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36531968-T-C

91410226-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36531968-T-G

91410240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36531982-C-T

91410249-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36531990-G-T

91410264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36532005-G-A

http://identifiers.org/hco/10/GRCh38#91410277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#36532018-C-A

91410277-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36532018-C-G

91410277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36532018-C-T

91410328-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36532071-C-G

91410328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36532071-C-T

91410398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36532143-G-A

91410398-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36532143-G-T

91410408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 36532153-G-A

91410408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 36532153-G-T

91410483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 36532228-G-A

91410483-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 36532228-G-C

91410483-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 36532228-G-T

http://identifiers.org/hco/10/GRCh38#91410499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36532244-C-A

91410499-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36532244-C-G

91410499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36532244-C-T

91410750-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36532402-G-C

91410786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36532437-C-T

91411019-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36532642-T-G

http://identifiers.org/hco/10/GRCh38#91411096-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36532719-A-C

91411100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36532723-A-G

91411148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36532773-G-A

91411148-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36532773-G-C

91411148-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36532773-G-T

91411198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36532818-A-G

http://identifiers.org/hco/10/GRCh38#91411225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36532847-C-A

91411855-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36533460-G-T

91412195-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36534013-G-C

91412390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36534162-A-G

http://identifiers.org/hco/10/GRCh38#91412664-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36534297-C-A

91412664-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36534297-C-G

91412767-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36534385-T-G

91412797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36534405-A-G

91413015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36534582-G-A

91413129-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36534705-C-G

91413142-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36534718-T-A

91413142-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36534718-T-G

http://identifiers.org/hco/10/GRCh38#91413498-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36535196-A-C

91413698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36535390-G-A

91414923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36536821-T-C

91414981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36536886-G-T

91415045-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36536950-G-T

91415380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36537387-A-G

91415380-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36537387-A-T

91415386-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36537393-C-G

91415386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36537393-C-T

http://identifiers.org/hco/10/GRCh38#91415503-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36537646-C-A

91415513-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36537656-G-C

91415594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36537734-A-G

91415600-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36537740-G-T

http://identifiers.org/hco/10/GRCh38#91415761-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36537863-C-A

91415761-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36537863-C-G

91415955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36538089-A-G

91416001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36538129-T-C

91416076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36538173-C-T

91416702-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36538424-G-T

91416791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36538499-A-G

91416933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36538597-T-C

91416938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36538602-A-G

91417147-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36538802-T-G

91417165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36538819-T-C

91417217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36538868-C-T

91418547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36540812-A-G

91418547-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36540812-A-T

http://identifiers.org/hco/10/GRCh38#91418678-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36540920-C-A

91418721-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36540944-C-G

91418971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36541199-A-G

91419112-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36541343-G-T

http://identifiers.org/hco/10/GRCh38#91419137-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36541368-A-C

91419221-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36541451-A-G

91419312-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36541526-C-G

91419370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36541577-A-G

91419386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36541593-A-G

http://identifiers.org/hco/10/GRCh38#91419414-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36541624-C-A

91419738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36541907-G-A

91419835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36542014-A-G

91421710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36542755-G-A

91421710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36542755-G-T

91421720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36542765-G-A

91421805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36542852-A-G

91423408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36544244-C-T

91423534-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36544348-G-C

91423534-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36544348-G-T

http://identifiers.org/hco/10/GRCh38#91423621-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36544750-A-C

http://identifiers.org/hco/10/GRCh38#91423830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36545165-C-A

91424032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36545349-A-G

91424111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36545429-A-G

91424114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36545432-C-T

91424152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36545472-C-T

91424245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36545561-G-A

91424312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36545641-G-A

91424576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36546198-T-C

91424579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36546201-G-A

91424579-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36546201-G-T

91424641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36546250-G-A

91424688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36546290-T-C

91424720-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36546321-C-G

91424762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36546348-C-T

91424938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36546514-C-T

91425129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36546685-T-C

91425136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36546692-A-G

91425159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36546715-G-A

91425358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 36546850-T-C

91426684-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36549601-T-A

91426755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36549671-A-G

91426778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36549694-A-G

91426793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36549710-C-T

91432032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36549862-G-A

91432414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36550259-A-G

91432484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36550327-A-G

91432491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36550337-T-C

91432981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36550937-G-A

91433203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36551136-G-A

91433378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36552037-A-G

91433539-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36552169-G-T

91433687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36552337-A-G

91433695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36552345-G-A

91433906-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36552550-A-T

91433950-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36552589-G-T

91433973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36552612-G-A

91434036-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36552645-A-T

91434040-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36552649-C-G

91434057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36552656-A-G

91434060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36552659-A-G

91434318-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36552907-C-G

91434332-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36552919-T-G

91434581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36553128-C-T

91435981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36554622-A-G

91436031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36554673-A-G

91436218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36554849-C-T

91436358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36554983-T-C

91436358-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36554983-T-G

91436384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36555011-A-G

91436452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36555095-T-C

91436986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36555585-C-T

91436995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36555594-A-G

91437062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36555885-G-A

91437719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36556456-T-C

91437787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36556506-T-C

91437800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36556520-A-G

91437864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36556583-G-A

91437869-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36556588-G-T

91444251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36558609-C-T

91444839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36558045-T-C

http://identifiers.org/hco/10/GRCh38#91445244-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36557658-C-A

91445316-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36557589-C-G

91445412-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36557509-T-A

91460170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36561092-G-A

91460326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36561242-A-G

91460370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36561281-T-C

91460386-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36561297-T-G

91460488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 36561397-A-G

91460492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36561401-T-C

http://identifiers.org/hco/10/GRCh38#91460512-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36561421-A-C

91460528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36561437-A-G

91460612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36561525-G-A

91460612-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36561525-G-C

91460612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36561525-G-T

91460644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36561557-A-G

91460668-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36561586-G-T

91460888-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36561797-A-T

91461021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36562051-A-G

91461104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36562133-T-C

91461118-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36562147-A-G

91461118-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36562147-A-T

http://identifiers.org/hco/10/GRCh38#91461151-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36562181-C-A

91461261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36562303-G-A

91461261-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36562303-G-C

91461284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 36562326-A-G

http://identifiers.org/hco/10/GRCh38#91461454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36562488-C-A

91461454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36562488-C-T

91461457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36562492-G-A

91461457-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36562492-G-T

91461948-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36562703-T-A

91461957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36562712-G-A

91461957-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36562712-G-C

91461957-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36562712-G-T

http://identifiers.org/hco/10/GRCh38#91462051-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36562800-C-A

91462106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 36562855-T-C

91462136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 36562885-G-A

91462136-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 36562885-G-T

91462337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36563325-T-C

91462365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36563348-G-A

91462365-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36563348-G-C

91462365-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36563348-G-T

91462398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36563381-T-C

91462398-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36563381-T-G

91462449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36563418-G-A

91477877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36564451-G-A

http://identifiers.org/hco/10/GRCh38#91478000-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36564562-A-C

91480832-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36572360-T-G

91480946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36572457-T-C

http://identifiers.org/hco/10/GRCh38#91480965-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36572486-A-C

91480975-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36572496-A-T

http://identifiers.org/hco/10/GRCh38#91480979-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36572500-C-A

91480979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36572500-C-T

http://identifiers.org/hco/10/GRCh38#91481002-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36572519-C-A

91481002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36572519-C-T

http://identifiers.org/hco/10/GRCh38#91481009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36572524-C-A

http://identifiers.org/hco/10/GRCh38#91481060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36572575-C-A

91481060-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36572575-C-G

91481204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36572703-A-G

91481204-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36572703-A-T

91481223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36572722-A-G

91481533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36572939-G-A

91482114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36573529-A-G

91482114-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36573529-A-T

91482380-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36573935-T-A

91482843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36574354-G-A

91482853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36574369-T-C

91482855-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36574371-T-G

91482873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36574389-T-C

http://identifiers.org/hco/10/GRCh38#91482887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36574403-C-A

91482887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36574403-C-T

http://identifiers.org/hco/10/GRCh38#91483032-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36574542-C-A

91483032-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 36574542-C-G

91483032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 36574542-C-T

91483193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36574706-A-G

91483218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36574731-A-G

91483225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36574738-T-C

91483529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36574993-A-G

http://identifiers.org/hco/10/GRCh38#91483694-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36575212-A-C

91483996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36575682-A-G

http://identifiers.org/hco/10/GRCh38#91484004-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36575690-C-A

91484004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36575690-C-T

91484013-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36575697-G-T

91484022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36575705-T-C

91484149-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36575909-T-G

http://identifiers.org/hco/10/GRCh38#91484214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36576015-C-A

91484214-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36576015-C-G

http://identifiers.org/hco/10/GRCh38#91484290-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36576076-C-A

91484349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36576130-A-G

91484480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36576260-T-C

91484567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 36576347-C-T

91484735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36576514-A-G

91484744-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36576523-T-A

91484744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36576523-T-C

91484773-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36576552-G-T

91484960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36576793-A-G

91484960-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36576793-A-T

91485135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36576951-T-C

http://identifiers.org/hco/10/GRCh38#91485309-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36577125-A-C

91485324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36577140-G-T

91485347-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36577161-T-A

91485347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36577161-T-C

http://identifiers.org/hco/10/GRCh38#91485372-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36577185-A-C

91485412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36577235-A-G

91486315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36577505-T-C

91486440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36577598-A-G

91486496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36577643-A-G

91486497-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36577644-G-C

91486792-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36577935-C-G

91486802-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36577942-T-G

91487025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36578195-A-G

http://identifiers.org/hco/10/GRCh38#91487098-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36578272-A-C

91487098-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36578272-A-T

http://identifiers.org/hco/10/GRCh38#91487100-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36578274-C-A

91487100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36578274-C-T

http://identifiers.org/hco/10/GRCh38#91487173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36578324-C-A

91487263-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36578409-A-T

91487282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36578428-C-T

http://identifiers.org/hco/10/GRCh38#91487356-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36578504-C-A

91487416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36578575-T-C

http://identifiers.org/hco/10/GRCh38#91487480-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36578640-C-A

91487614-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36578767-G-C

91487614-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36578767-G-T

91487791-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36578941-T-A

91487791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36578941-T-C

http://identifiers.org/hco/10/GRCh38#91487854-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36578998-C-A

91487854-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36578998-C-G

http://identifiers.org/hco/10/GRCh38#91487882-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36579027-A-C

91487882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36579027-A-G

91488041-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36579167-G-C

91488051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36579178-G-A

91488127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36579213-T-C

http://identifiers.org/hco/10/GRCh38#91488146-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36579232-A-C

http://identifiers.org/hco/10/GRCh38#91488368-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36579424-C-A

91488788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36579777-G-A

91488788-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36579777-G-T

http://identifiers.org/hco/10/GRCh38#91488851-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36579840-C-A

91488936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36579900-A-G

91488956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36579922-T-C

91488972-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36579938-T-A

91489153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36580087-G-T

http://identifiers.org/hco/10/GRCh38#91489226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36580135-C-A

91489226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36580135-C-T

http://identifiers.org/hco/10/GRCh38#91489234-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36580140-C-A

91489234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36580140-C-T

91489235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36580141-G-A

91489320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36580199-C-T

91489513-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36580339-A-T

91489547-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36580368-C-G

91489568-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36580388-A-T

91489634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36580448-C-T

http://identifiers.org/hco/10/GRCh38#91489671-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36580489-C-A

91489695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36580512-A-G

91489707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36580524-T-C

91489721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36580548-G-A

91490527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36581222-G-A

91490620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36581303-G-A

91490624-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36581307-G-C

http://identifiers.org/hco/10/GRCh38#91490627-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36581310-C-A

91490627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36581310-C-T

91491076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36581528-A-G

91491172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36581621-A-G

91491333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36581783-A-G

91491334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36581784-A-G

91491334-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36581784-A-T

http://identifiers.org/hco/10/GRCh38#91491346-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36581796-A-C

91491418-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36581839-T-C

91491612-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36581982-T-G

http://identifiers.org/hco/10/GRCh38#91492282-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36582500-C-A

91492282-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36582500-C-G

91492282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36582500-C-T

91492307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36582523-T-C

91492307-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36582523-T-G

http://identifiers.org/hco/10/GRCh38#91492328-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36582544-C-A

91492519-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36582710-T-A

91492544-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36582724-G-T

http://identifiers.org/hco/10/GRCh38#91492550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36582730-C-A

91492550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36582730-C-T

91492586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36582739-T-C

http://identifiers.org/hco/10/GRCh38#91492590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36582743-C-A

91492590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36582743-C-T

http://identifiers.org/hco/10/GRCh38#91492591-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36582744-C-A

91492868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36582934-T-C

91493213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36583601-A-G

91493292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36583685-A-G

http://identifiers.org/hco/10/GRCh38#91493303-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36583696-C-A

91493559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36583925-A-G

91493627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36583985-A-G

http://identifiers.org/hco/10/GRCh38#91493689-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36584051-A-C

91493796-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36584135-A-T

91494190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36584547-G-A

91494384-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36584766-G-C

91494423-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36584807-G-T

91494430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36584814-A-G

91494603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36584960-C-T

91494677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36585032-A-G

91494684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36585040-A-G

http://identifiers.org/hco/10/GRCh38#91494734-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36585087-A-C

91494796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36585130-T-C

91494797-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36585131-A-T

91494807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36585141-T-C

91494893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36585226-A-G

91496121-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36586586-G-C

91496121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36586586-G-T

91496142-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36586593-G-C

91496142-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36586593-G-T

91496403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36586854-T-C

91496455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36586895-T-C

91496473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36586913-G-A

91496473-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36586913-G-T

91496484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36586919-C-T

http://identifiers.org/hco/10/GRCh38#91496485-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36586920-C-A

91496513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36586948-A-G

91496520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36586955-T-C

91497627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36588272-T-C

91497707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36588346-C-T

91497750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36588389-G-A

91497750-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36588389-G-C

91497750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36588389-G-T

91497957-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36588588-G-T

91498036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36588677-T-C

91498055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36588701-T-C

91498092-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36588748-A-T

91498123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 36588779-T-C

91498283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36588930-T-C

91498399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36589170-T-C

91498510-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36589268-G-C

91498682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36589386-A-G

http://identifiers.org/hco/10/GRCh38#91498723-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36589418-A-C

91498781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36589472-A-G

91498781-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36589472-A-T

91498980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36589653-A-G

91499129-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 36589802-G-C

http://identifiers.org/hco/10/GRCh38#91499159-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36589832-A-C

91499165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36589838-T-C

91499174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36589842-G-A

91499174-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36589842-G-C

91499178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36589846-T-C

91499192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36589860-T-C

91499196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36589864-A-G

91499234-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36589897-G-C

91499234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36589897-G-T

91499301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36590119-C-T

91499382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36590204-G-A

91499541-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36590318-A-T

91499620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36590382-G-A

http://identifiers.org/hco/10/GRCh38#91499675-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36590426-C-A

91499787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36590717-C-T

91499824-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36590753-G-T

91499985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36591108-G-A

91500025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36591146-T-C

http://identifiers.org/hco/10/GRCh38#91500155-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36591269-A-C

91500155-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36591269-A-T

91500220-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36591311-A-T

91500238-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36591326-G-C

91500281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36591369-C-T

91500398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36591480-A-G

91500398-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36591480-A-T

http://identifiers.org/hco/10/GRCh38#91500403-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36591485-A-C

91500403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36591485-A-G

91500403-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36591485-A-T

91500432-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36591518-G-T

http://identifiers.org/hco/10/GRCh38#91500459-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36591545-C-A

91500459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36591545-C-T

91500588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 36591834-T-C

91500737-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36592531-G-T

91500989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36592777-T-C

91501197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 36592906-T-C

91501472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36593402-G-A

91501472-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36593402-G-C

91502134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36594016-C-T

http://identifiers.org/hco/10/GRCh38#91502528-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36594331-C-A

91502633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36594729-C-T

91502756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36594877-T-C

91511430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36595748-A-G

91511928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36595823-T-C

91512178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36596042-T-C

91512228-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36596084-C-G

91512242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36596098-T-C

http://identifiers.org/hco/10/GRCh38#91512449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36596308-C-A

91512449-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36596308-C-G

91512449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36596308-C-T

91512583-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36596460-G-T

91512605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36596476-G-A

91512622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 36596493-G-A

91512622-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 36596493-G-C

91512622-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 36596493-G-T

http://identifiers.org/hco/10/GRCh38#91512639-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36596510-C-A

91512639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36596510-C-T

http://identifiers.org/hco/10/GRCh38#91512675-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36596547-A-C

91512675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36596547-A-G

91513302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36597154-A-G

91513798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36597650-C-T

91514014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36597847-G-A

91514477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36598269-C-T

91514508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26736
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36598297-A-G