81007562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83527477-T-C

81007562-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83527477-T-G

81008252-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83526555-A-T

81008451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83526186-G-A

81008451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83526186-G-T

81008510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83526121-C-T

81009376-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83525642-A-T

http://identifiers.org/hco/15/GRCh38#81009562-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83525276-A-C

81009841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83524901-C-T

81009934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83524634-G-A

http://identifiers.org/hco/15/GRCh38#81010019-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83524567-A-C

81011778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83524091-G-A

81011929-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83523960-A-T

81012087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83523834-A-G

81012196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83523738-T-C

81012681-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83523594-G-T

http://identifiers.org/hco/15/GRCh38#81012879-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83523408-A-C

81012939-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83523352-A-T

81012943-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83523347-G-C

81012970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83523321-T-C

81012999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83523292-A-G

81013151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83523181-A-G

81013253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83523077-C-T

81013313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83523019-A-G

81013340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83522991-C-T

81013508-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83522843-G-T

81013557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83522798-C-T

81013568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83522788-C-T

81013596-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83522760-G-T

81014391-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83522213-T-A

81014391-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83522213-T-C

81014424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83522180-T-C

81014484-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83522107-T-A

81015981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83519268-A-G

81015981-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83519268-A-T

81016179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83519064-G-A

81016179-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83519064-G-T

81016349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83518696-C-T

81016382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83518669-A-G

81016755-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83517710-A-T

http://identifiers.org/hco/15/GRCh38#81017095-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83517370-A-C

81017095-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83517370-A-T

81020107-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83513322-A-T

81020217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83513227-A-G

81020218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83513226-G-A

81020240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83513184-A-G

81020254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83513170-G-A

81020306-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83513086-C-G

81020328-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83513064-T-G

81020403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83513037-A-G

81020447-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83512993-C-G

81021433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83511092-C-T

81021578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83510950-A-G

81023825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83508857-G-A

81023960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83508682-G-A

81024152-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83508217-C-G

81024152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83508217-C-T

81024309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83508069-G-A

81024310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83508068-G-A

81024411-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83507974-G-C

81024583-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83507820-G-C

81024692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83507717-G-A

81025830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83506123-C-T

81026058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83505900-G-A

81026286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83505669-A-G

81026318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83505638-A-G

81026320-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83505636-G-T

81026354-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83505602-T-G

81030484-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83501379-A-T

81031019-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83499050-T-G

81031984-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83498578-G-C

81031990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83498572-G-A

81031990-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83498572-G-C

81031990-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83498572-G-T

81033058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83496974-T-C

81033366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83496692-A-G

81033449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83496589-C-T

81033453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83496585-C-T

81033531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83496430-T-C

81033619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83496369-C-T

http://identifiers.org/hco/15/GRCh38#81033637-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83496351-C-A

81033737-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83496262-C-G

81033801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83496199-A-G

81033872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83496131-C-T

81033908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83496095-A-G

81034097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83495912-T-C

81035679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: -G-A

81037082-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83493891-G-C

81037147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83493827-T-C

81037167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83493814-G-A

81039272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83492446-T-C

81039322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83492396-T-C

81039442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83492276-T-C

81040041-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83491709-A-T

81040120-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83491646-G-C

81040213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83491311-C-T

81040271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83491239-A-G

81040511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83491016-T-C

81040545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83490985-A-G

81041095-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83490798-T-A

81041346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83490528-A-G

81041847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83489950-A-G

81042201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83489641-T-C

81042230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83489613-T-C

81042230-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83489613-T-G

81042300-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83489552-C-G

http://identifiers.org/hco/15/GRCh38#81042350-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83489510-A-C

81042526-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83489341-T-G

81061111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron_variant, undefined
orthologous variants: 83487718-A-G

81061112-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron_variant, undefined
orthologous variants: 83487717-T-G

http://identifiers.org/hco/15/GRCh38#81061114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#83487715-C-A

81061210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron_variant, undefined
orthologous variants: 83487627-G-A

81061210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron_variant, undefined
orthologous variants: 83487627-G-T

http://identifiers.org/hco/15/GRCh38#81061251-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#83487598-A-C

81061251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron_variant, undefined
orthologous variants: 83487598-A-G

81061425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron_variant, undefined
orthologous variants: 83487441-T-C

http://identifiers.org/hco/15/GRCh38#81061475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#83487392-C-A

81061475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron_variant, undefined
orthologous variants: 83487392-C-T

81061759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron_variant, undefined
orthologous variants: 83487137-G-T

http://identifiers.org/hco/15/GRCh38#81061784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#83487112-C-A

http://identifiers.org/hco/15/GRCh38#81061791-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#83487105-C-A

81061805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron_variant, undefined
orthologous variants: 83487089-G-A

81061827-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron_variant, undefined
orthologous variants: 83487068-A-T

81062203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron_variant, undefined
orthologous variants: 83486666-T-C

81062277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron_variant, undefined
orthologous variants: 83486608-A-G

81062330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron_variant, undefined
orthologous variants: 83486559-G-A

81062343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron_variant, undefined
orthologous variants: 83486546-G-T

81062357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron_variant, undefined
orthologous variants: 83486532-G-A

81062363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron_variant, undefined
orthologous variants: 83486526-A-G

81062506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron_variant, undefined
orthologous variants: 83486402-G-A

81062506-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron_variant, undefined
orthologous variants: 83486402-G-T

http://identifiers.org/hco/15/GRCh38#81062514-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#83486394-A-C

81063791-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83485027-G-C

81064083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83484700-G-A

81064095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83484687-A-G

81064145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83484649-A-G

81064256-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83484543-T-G

81064314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83484486-C-T

81064315-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83484485-G-C

81064492-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83484359-A-T

81064629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83484248-C-T

81064631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83484246-C-T

81064653-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83484225-C-G

81065212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83484002-G-A

81065212-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83484002-G-T

81065253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83483958-G-A

81065268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83483944-T-C

81065275-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83483937-G-T

81065320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83483895-G-A

81065324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83483891-T-C

81065361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83483858-G-A

81065370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83483849-G-A

81065406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83483816-A-G

81065418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83483804-C-T

81065474-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83483749-A-T

81071021-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83480495-T-A

81071021-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83480495-T-G

81071525-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83480038-G-T

81073347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83479360-G-A

81073617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83479173-A-G

81073688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83479102-C-T

81073702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83479088-T-C

81073702-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83479088-T-G

81073731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83479058-G-A

81073821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron_variant, undefined
orthologous variants: 83478974-A-G

81073887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83478916-G-A

81073965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83478831-T-C

http://identifiers.org/hco/15/GRCh38#81073993-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83478807-A-C

81074017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83478783-C-T

81074178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83478421-A-G

81074251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83478218-T-C

81074280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83478189-A-G

81074518-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83477979-G-C

81074518-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83477979-G-T

81074523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83477974-G-A

81074597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83477899-G-A

81074602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83477894-T-C

81074628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83477865-G-A

81074842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83477643-A-G

81074907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83477563-T-C

81074925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83477545-C-T

81074962-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83477510-C-G

81074962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83477510-C-T

81074998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83477475-A-G

81075007-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83477466-T-A

81075110-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83477369-T-A

81080979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron_variant, undefined
orthologous variants: 83474049-G-A

81081048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron_variant, undefined
orthologous variants: 83473982-G-A

81081144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron_variant, undefined
orthologous variants: 83473866-G-A

81081149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: 83473861-T-C

81081152-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: 83473858-T-A

81081230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron_variant, undefined
orthologous variants: 83473778-G-A

81081898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron_variant, undefined
orthologous variants: 83473146-C-T

81081899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron_variant, undefined
orthologous variants: 83473145-T-C

81083638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83471748-C-T

81083665-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83471722-A-T

81083669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83471718-C-T

81083816-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83471622-T-A

81083816-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83471622-T-G

81083818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83471620-G-A

81083818-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83471620-G-C

81083982-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83471458-C-G

81083982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83471458-C-T

81084382-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83471067-T-A

81084499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83470970-A-G

http://identifiers.org/hco/15/GRCh38#81084973-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83470373-C-A

81085059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83470300-A-G

81085110-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83470249-G-C

81085243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83470114-G-A

81085281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83470076-G-A

81085331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83470031-C-T

81085336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83470026-C-T

81085431-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83469949-C-G

81085480-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83469899-C-G

81085524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83469840-C-T

http://identifiers.org/hco/15/GRCh38#81085560-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83469804-C-A

81088241-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83467816-T-G

81088602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83467503-G-A

81088742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83467371-C-T

81088840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83467296-C-T

81089310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83467075-T-C

81089640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83465517-G-A

81089643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83465514-G-A

81089827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83465349-G-A

81090577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83463998-C-T

81090804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83463783-A-G

81090832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83463755-A-G

81092151-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83463520-C-G

81092334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron_variant, undefined
orthologous variants: 83463354-C-T

81092523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83463170-T-C

81092574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron_variant, undefined
orthologous variants: 83463112-G-A

81097839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83461211-C-T

81097857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83461193-C-T

81097951-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83461104-T-A

81098225-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83460412-G-C

81098642-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83460200-T-A

81098844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83460040-A-G

81098880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83460003-T-C

http://identifiers.org/hco/15/GRCh38#81099330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83459571-C-A

81099330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83459571-C-T

81099334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83459567-A-G

http://identifiers.org/hco/15/GRCh38#81099399-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#83459506-C-A

81101627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83458769-A-G

81101787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83458652-T-C

http://identifiers.org/hco/15/GRCh38#81102000-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83458432-A-C

81102192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83458253-G-A

81102727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83458026-G-A

81102727-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83458026-G-T

81102735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83458018-G-T

http://identifiers.org/hco/15/GRCh38#81102873-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83457698-A-C

81102873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83457698-A-G

http://identifiers.org/hco/15/GRCh38#81102950-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83457609-A-C

81102965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83457594-G-A

81102977-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83457580-C-G

81103124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83457456-G-A

http://identifiers.org/hco/15/GRCh38#81104101-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83457310-C-A

81105856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83453241-A-G

81106040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83453068-A-G

81106150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83452956-T-C

81106201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83452908-A-G

81106464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83452535-C-T

81106492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron_variant, undefined
orthologous variants: 83452508-T-C

81106596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83452403-A-G

81106677-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron_variant, undefined
orthologous variants: 83451928-T-A

81106717-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron_variant, undefined
orthologous variants: 83451889-G-T

81107122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83451801-T-C

81107162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83451762-C-T

81108334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83451019-G-A

81108424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83450939-G-A

81108499-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83450882-G-T

81108678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83450730-A-G

81110277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83450656-C-T

81110283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83450650-T-C

81110346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83450598-G-A

81110445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83450523-A-G

81110640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83450301-T-C

81110681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83450236-G-A

http://identifiers.org/hco/15/GRCh38#81110787-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83450139-A-C

81111025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83449907-A-G

81111100-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83449832-G-C

81111146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83449795-C-T

81111217-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83449733-C-G

81111288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83449664-C-T

81111355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83449626-A-G

81111400-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83449582-C-G

81111414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83449568-C-T

http://identifiers.org/hco/15/GRCh38#81111557-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83449447-C-A

81111638-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83449382-T-G

81111656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83449364-A-G

81111777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83449210-G-A

81111929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83447955-C-T

81112066-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83447822-T-G

81112150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83447736-A-G

81133025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83445292-A-G

http://identifiers.org/hco/15/GRCh38#81133119-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83445203-C-A

81133124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83445198-T-C

http://identifiers.org/hco/15/GRCh38#81133171-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83445167-A-C

81133171-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83445167-A-T

81133432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83445069-A-G

81133436-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83445065-T-G

81133567-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83444946-C-G

81134055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83444282-T-C

81134067-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83444268-A-T

81134099-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83444219-C-G

81134099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83444219-C-T

81134111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron_variant, undefined
orthologous variants: 83444207-G-A

81134111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron_variant, undefined
orthologous variants: 83444207-G-T

81134130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83444188-G-A

81134134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83444181-G-A

81134134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83444181-G-T

http://identifiers.org/hco/15/GRCh38#81134205-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#83444150-C-A

81134205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron_variant, undefined
orthologous variants: 83444150-C-T

http://identifiers.org/hco/15/GRCh38#81134209-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83444146-C-A

81134209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83444146-C-T

81134273-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 83444078-G-C

81134284-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 83444067-A-T

81134293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 83444058-G-T

81134294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 83444057-T-C

81134327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 83444019-G-A

81134327-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 83444019-G-C

81134327-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 83444019-G-T

81134340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 83444006-A-G

81134345-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 83444001-T-A

81134345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 83444001-T-C

81134387-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron_variant, missense_variant
orthologous variants: 83443959-T-G

81134396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron_variant, missense_variant, splice_region_variant
orthologous variants: 83443950-G-A

http://identifiers.org/hco/15/GRCh38#81134494-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83443880-C-A

81134494-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83443880-C-G

81134494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83443880-C-T

81134516-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83443859-T-A

http://identifiers.org/hco/15/GRCh38#81134526-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83443855-A-C

81134526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83443855-A-G

http://identifiers.org/hco/15/GRCh38#81134532-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83443849-C-A

81134532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83443849-C-T

81134877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83443675-C-T

81134986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83443588-G-A

http://identifiers.org/hco/15/GRCh38#81135140-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83443429-C-A

81135140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83443429-C-T

81135192-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83443381-G-T

81135303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: missense variant
orthologous variants: 83443258-A-G

81136163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83442991-C-T

81136239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83442912-A-G

81136378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83442794-A-G

81136437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83442741-G-A

81136474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83442691-G-A

81136474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83442691-G-T

81136479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83442686-G-A

81136479-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83442686-G-T

81136559-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: missense variant
orthologous variants: 83442607-A-T

81136657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: missense variant
orthologous variants: 83442506-T-C

81136773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83442392-C-T

81136798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83442371-T-C

81136891-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83442283-T-A

81136891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83442283-T-C

81136891-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83442283-T-G

81136920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83442267-A-G

81137093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83442076-G-A

81137108-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83442061-A-T

81137318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83441909-G-T

81137436-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83441775-A-T

81137831-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83441465-G-C

http://identifiers.org/hco/15/GRCh38#81138177-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83440798-C-A

81138177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83440798-C-T

http://identifiers.org/hco/15/GRCh38#81138201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83440775-C-A

81138201-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83440775-C-G

http://identifiers.org/hco/15/GRCh38#81138303-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83440694-C-A

81138304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83440693-A-G

81139854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83432475-G-T

81139980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83432375-A-G

81140043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83432325-T-C

81140813-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83431533-C-G

81141201-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83431145-A-T

81141237-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83431109-T-A

81142889-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83430300-G-T

81143062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83430164-C-T

81143536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83429639-T-C

81143743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: missense variant
orthologous variants: 83429447-G-A

81143743-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: missense variant
orthologous variants: 83429447-G-T

81143790-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: missense variant
orthologous variants: 83429400-A-T

81143844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83429346-T-C

81143844-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83429346-T-G

81143851-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83429339-C-G

81143851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83429339-C-T

81144817-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83428655-G-C

81144901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83428595-C-T

81145244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83428297-T-C

81145383-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83428167-G-C

http://identifiers.org/hco/15/GRCh38#81145800-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83427886-A-C

81146053-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83427453-G-C

81147847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83426363-T-C

81148175-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83425552-A-T

81148200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83425527-A-G

81148322-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: intron variant
orthologous variants: 83425396-T-G

81148357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: missense variant
orthologous variants: 83425349-G-A

81148357-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: missense variant
orthologous variants: 83425349-G-C

http://identifiers.org/hco/15/GRCh38#81148492-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83425214-A-C

http://identifiers.org/hco/15/GRCh38#81148578-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83425128-A-C

http://identifiers.org/hco/15/GRCh38#81148600-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83425105-C-A

81148600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: 3 prime UTR variant
orthologous variants: 83425105-C-T

81148630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: 3 prime UTR variant
orthologous variants: 83425071-A-G

81148630-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: 3 prime UTR variant
orthologous variants: 83425071-A-T

81148673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: 3 prime UTR variant
orthologous variants: 83425029-T-C

81148813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: 3 prime UTR variant
orthologous variants: 83424904-A-G

81148813-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: 3 prime UTR variant
orthologous variants: 83424904-A-T

81148838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26782
most severe consequence: 3 prime UTR variant
orthologous variants: 83424873-G-A