86201310-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: 5 prime UTR variant
orthologous variants: 89671087-C-G

86201702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron variant
orthologous variants: 89670382-G-A

86201936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron variant
orthologous variants: 89670230-T-C

86201959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron variant
orthologous variants: 89670228-C-T

86201960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron variant
orthologous variants: 89670227-A-G

86202141-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron variant
orthologous variants: 89670084-T-A

86202259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron variant
orthologous variants: 89669868-G-T

86202369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron variant
orthologous variants: 89669780-C-T

86202408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron variant
orthologous variants: 89669752-A-G

86203176-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron variant
orthologous variants: 89668833-C-G

http://identifiers.org/hco/11/GRCh38#86203222-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89668788-A-C

86203485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron variant
orthologous variants: 89668302-G-A

86206384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron variant
orthologous variants: 89665597-T-C

86206388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron variant
orthologous variants: 89665593-A-G

86206494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron variant
orthologous variants: 89665506-G-A

86208526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron variant
orthologous variants: 89663357-C-T

86208640-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron variant
orthologous variants: 89663243-G-C

86208647-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron variant
orthologous variants: 89663236-T-G

86208805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron variant
orthologous variants: 89663132-G-A

86208997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron variant
orthologous variants: 89662731-T-C

86209045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron variant
orthologous variants: 89662683-A-G

86209147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron variant
orthologous variants: 89662608-A-G

86209286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron variant
orthologous variants: 89662479-C-T

86209562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron variant
orthologous variants: 89662091-A-G

86209563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron variant
orthologous variants: 89662090-G-A

86209660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron variant
orthologous variants: 89661979-T-C

86211724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron variant
orthologous variants: 89661104-G-A

86212399-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron variant
orthologous variants: 89660857-A-T

86212874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron variant
orthologous variants: 89659465-A-G

http://identifiers.org/hco/11/GRCh38#86212904-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89659435-A-C

86213076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron variant
orthologous variants: 89659276-T-C

86213286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron variant
orthologous variants: 89658920-G-A

86213462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron variant
orthologous variants: 89658738-A-G

86214518-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron variant
orthologous variants: 89657038-G-C

86214608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron variant
orthologous variants: 89656949-T-C

86214696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, undefined
orthologous variants: 89656854-T-C

http://identifiers.org/hco/11/GRCh38#86214733-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#89656818-C-A

86214810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, undefined
orthologous variants: 89656734-G-A

86214881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, undefined
orthologous variants: 89656662-A-G

86215731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron variant
orthologous variants: 89655340-G-A

http://identifiers.org/hco/11/GRCh38#86217584-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89648432-A-C

86217599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron variant
orthologous variants: 89648417-C-T

86217765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron variant
orthologous variants: 89648362-C-T

86218069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron variant
orthologous variants: 89647897-T-C

86218084-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron variant
orthologous variants: 89647883-A-T

86218197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron variant
orthologous variants: 89647787-T-C

86218197-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron variant
orthologous variants: 89647787-T-G

86218220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron variant
orthologous variants: 89647763-G-A

http://identifiers.org/hco/11/GRCh38#86218276-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89647708-A-C

86218276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron variant
orthologous variants: 89647708-A-G

86218323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron variant
orthologous variants: 89647663-T-C

86218587-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, undefined
orthologous variants: 89647457-A-T

86218691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, undefined
orthologous variants: 89647361-A-G

http://identifiers.org/hco/11/GRCh38#86218731-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#89647320-C-A

86218731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, undefined
orthologous variants: 89647320-C-T

http://identifiers.org/hco/11/GRCh38#86218958-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89645985-C-A

86219126-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron variant
orthologous variants: 89645815-C-G

http://identifiers.org/hco/11/GRCh38#86219213-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89645736-A-C

86219430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron variant
orthologous variants: 89645523-A-G

86220054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron variant
orthologous variants: 89644100-G-A

86220054-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron variant
orthologous variants: 89644100-G-T

86220060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron variant
orthologous variants: 89644094-A-G

86220087-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron variant
orthologous variants: 89644065-A-T

86220317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron variant
orthologous variants: 89643897-C-T

86220379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron variant
orthologous variants: 89643844-A-G

86220572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron variant
orthologous variants: 89643624-A-G

86220584-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron variant
orthologous variants: 89643470-A-T

86220790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron variant
orthologous variants: 89643261-C-T

86220934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron variant
orthologous variants: 89643125-A-G

86221962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron variant
orthologous variants: 89642614-G-A

86222064-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron variant
orthologous variants: 89642509-T-A

86222162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron variant
orthologous variants: 89642413-A-G

86222238-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron variant
orthologous variants: 89642351-T-G

86222307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron variant
orthologous variants: 89642284-T-C

86222311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron variant
orthologous variants: 89642280-C-T

86222424-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron variant
orthologous variants: 89642167-A-T

86222590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron variant
orthologous variants: 89642000-A-G

86228888-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron variant
orthologous variants: 89639299-T-A

86229036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron variant
orthologous variants: 89639157-G-A

86229465-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron variant
orthologous variants: 89639105-G-C

http://identifiers.org/hco/11/GRCh38#86229700-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89638916-A-C

86229705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron variant
orthologous variants: 89638911-G-A

86229705-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron variant
orthologous variants: 89638911-G-C

86229705-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron variant
orthologous variants: 89638911-G-T

http://identifiers.org/hco/11/GRCh38#86230624-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89637563-A-C

86230671-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron variant
orthologous variants: 89637521-C-G

86230693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron variant
orthologous variants: 89637502-T-C

86234321-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron variant
orthologous variants: 89633465-T-C

86234702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron variant
orthologous variants: 89633134-A-G

86235183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron variant
orthologous variants: 89632840-A-G

86235250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron variant
orthologous variants: 89632806-G-A

86235279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron variant
orthologous variants: 89632782-A-G

86235363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron variant
orthologous variants: 89632711-C-T

86235505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron variant
orthologous variants: 89632585-T-C

86235529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron variant
orthologous variants: 89632559-G-A

86244402-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 89630564-G-C

86244449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 89630518-T-C

86244471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 89630496-A-G

86244472-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 89630495-G-T

86244479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 89630488-G-A

86244480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 89630487-G-T

86244485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 89630481-G-A

86244485-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 89630481-G-C

86244485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 89630481-G-T

http://identifiers.org/hco/11/GRCh38#86244492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89630473-C-A

86244607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 89630358-A-G

http://identifiers.org/hco/11/GRCh38#86244622-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89630341-A-C

86244622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 89630341-A-G

86244636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 89630327-T-C

86244643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 89630320-G-A

86244662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 89630300-T-C

86244701-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 89630260-A-T

86244732-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 89630229-G-T

86244870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 89630094-T-C

86244948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 89630012-T-C

http://identifiers.org/hco/11/GRCh38#86245028-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89629932-C-A

86245028-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89629932-C-G

86245028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89629932-C-T

86245057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 89629901-G-A

86245057-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 89629901-G-C

86245057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 89629901-G-T

86245108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 89629850-G-A

86245108-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 89629850-G-C

86245108-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 89629850-G-T

86245328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 89629633-C-T

86245396-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89629566-T-A

86245396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89629566-T-C

http://identifiers.org/hco/11/GRCh38#86245454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89629501-C-A

86245454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89629501-C-T

86245455-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89629500-T-A

86245455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89629500-T-C

http://identifiers.org/hco/11/GRCh38#86245563-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89629393-C-A

86245563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89629393-C-T

86245708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89629237-G-A

86249345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89627460-G-A

86249402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89627412-T-C

86249403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89627411-T-C

86249444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89627357-G-A

86249444-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89627357-G-C

86250105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89626663-A-G

86250253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89626301-G-A

86250253-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89626301-G-C

86250311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 89626240-A-G

86250344-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 89626207-A-G

86250484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89626084-A-G

86250655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89625941-G-A

86250819-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89625776-A-T

86251104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89623384-G-A

86251118-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89623367-A-G

http://identifiers.org/hco/11/GRCh38#86251205-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89623299-A-C

http://identifiers.org/hco/11/GRCh38#86251233-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89623273-C-A

86251233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89623273-C-T

86251249-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89623257-A-T

86251353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89623171-G-A

86251516-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89622831-T-A

86251522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89622826-A-G

86252010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89622062-G-A

86252010-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89622062-G-T

86252035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89621649-T-C

86252038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89621646-A-G

86252045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89621639-A-G

86252046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89621638-A-G

86252205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 89621472-G-A

http://identifiers.org/hco/11/GRCh38#86252281-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89621397-C-A

86252281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89621397-C-T

86252284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89621394-A-G

86252301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89621386-T-C

86252301-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89621386-T-G

86252336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89621352-A-G

86252338-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89621350-G-T

86252356-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89621332-T-G

86255024-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89621137-G-C

86255060-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89621102-T-G

86255070-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89621090-T-A

http://identifiers.org/hco/11/GRCh38#86255108-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89621070-A-C

86255108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89621070-A-G

86255108-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89621070-A-T

86255122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89621056-T-C

86255158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89620917-A-G

86255276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 89620757-G-A

86255276-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 89620757-G-C

86255300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89620733-G-T

86255327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89620705-A-G

86255327-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89620705-A-T

86255338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89620700-A-G

86255362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89620677-A-G

86255422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89620629-A-G

86255422-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89620629-A-T

86255433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89620617-T-C

86255462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89620608-T-C

86255521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89620549-G-T

86255546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89620531-T-C

http://identifiers.org/hco/11/GRCh38#86255628-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89620451-C-A

86255681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89620409-T-C

86255803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89620313-A-G

86255950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89620161-T-C

86256020-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89620116-G-T

86256056-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89620079-G-T

86256117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89620015-C-T

86256139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89619993-A-G

86256165-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89619967-C-G

http://identifiers.org/hco/11/GRCh38#86256238-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89619796-C-A

86256238-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89619796-C-G

86256238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89619796-C-T

86256242-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89619792-T-A

http://identifiers.org/hco/11/GRCh38#86256304-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89619725-C-A

86256304-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89619725-C-G

86256304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89619725-C-T

http://identifiers.org/hco/11/GRCh38#86256316-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89619713-A-C

86256316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89619713-A-G

86256444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 89619580-C-T

86256537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89619488-G-A

86256537-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89619488-G-C

86256537-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89619488-G-T

86256544-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89619480-T-G

86256597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89619426-G-A

86256597-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89619426-G-C

86256597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89619426-G-T

86256598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89619425-T-C

86256628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89619393-A-G

86256628-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89619393-A-T

86257195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89619345-G-A

86257243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89619297-G-T

86257276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89619235-G-A

86257276-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89619235-G-T

86257358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89619099-T-C

86257364-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89619093-T-A

http://identifiers.org/hco/11/GRCh38#86257443-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89618927-C-A

86257443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89618927-C-T

http://identifiers.org/hco/11/GRCh38#86264135-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89617047-A-C

86264347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89616835-T-C

86264782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89615628-A-G

86264788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89615623-T-C

86264936-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89615509-T-G

86265772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89614693-G-A

86265854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89614626-T-C

86265942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89614559-T-C

86265969-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89614532-T-A

86265995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89614159-G-A

86266255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89613885-G-A

86266255-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89613885-G-T

86266325-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89613863-T-G

86266561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89613594-A-G

86266561-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89613594-A-T

86266674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89613306-A-G

86267193-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89612757-G-C

86268642-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89611368-T-A

86268650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89611360-T-C

http://identifiers.org/hco/11/GRCh38#86268988-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89611059-A-C

86269495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89610630-C-T

86269530-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89610562-T-G

86270066-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89609817-G-T

86270072-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89609811-C-G

http://identifiers.org/hco/11/GRCh38#86270146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89609743-C-A

86270146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89609743-C-T

86270187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89609708-T-C

86270288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89609618-A-G

86270288-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89609618-A-T

86276115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89606275-A-G

86276141-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89606249-C-G

86276236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89606160-A-G

86276307-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89606129-G-C

86276307-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89606129-G-T

86276314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89606122-A-G

http://identifiers.org/hco/11/GRCh38#86276496-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89605978-A-C

86276543-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89605931-T-A

86276666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89605864-T-C

86276684-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89605846-G-T

86276688-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89605842-A-T

86276767-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89605794-G-T

86276809-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89605752-G-T

86276850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89605716-G-A

86276850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89605716-G-T

86276925-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89605662-G-T

http://identifiers.org/hco/11/GRCh38#86276952-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89605641-C-A

86276952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89605641-C-T

86277199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89605409-G-A

86277199-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89605409-G-T

http://identifiers.org/hco/11/GRCh38#86277287-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89605363-C-A

86277376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89605299-A-G

86277618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89605093-A-G

86277666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89605050-T-C

86277840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89604884-G-A

86277840-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89604884-G-T

86278025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89604700-G-A

86278144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89604627-A-G

http://identifiers.org/hco/11/GRCh38#86278162-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89604615-A-C

86278162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89604615-A-G

http://identifiers.org/hco/11/GRCh38#86278260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89604518-C-A

86278292-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3188
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89604427-T-A