10545616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110443836-A-G

http://identifiers.org/hco/11/GRCh38#10545658-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#110443870-A-C

10545801-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110444032-T-A

10546320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110444820-C-T

10546321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110444821-G-A

10546321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110444821-G-T

10546335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110444826-A-G

10546357-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110444837-G-C

10546876-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110445435-T-G

10547114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110446398-A-G

10547810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110446744-T-C

10548049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110447168-C-T

10548364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110447457-A-G

10548424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110447516-A-G

10548603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110447656-A-G

http://identifiers.org/hco/11/GRCh38#10549004-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#110448100-C-A

10549499-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110448262-T-G

10549507-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110448270-T-G

10549600-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110448355-T-G

10550711-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110448474-C-G

10550770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110448532-T-C

10550866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110448624-C-T

10550878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110448636-A-G

10551160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110449096-C-T

10557691-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110449677-T-A

10557808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110449764-G-T

http://identifiers.org/hco/11/GRCh38#10558149-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#110450229-A-C

10558250-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110450504-T-G

10558290-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110450555-A-G

10558416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110450791-A-G

10558416-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110450791-A-T

10558458-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110450818-A-T

10558472-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110450832-G-T

10558526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110450888-T-C

10558528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110450890-G-A

10558528-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110450890-G-C

10558584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110450951-C-T

10558883-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110451214-G-T

10558895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110451225-G-A

10558940-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110451267-T-G

10559089-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110451357-T-G

10559182-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110451450-T-G

10559246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110451514-G-A

10559246-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110451514-G-C

10559246-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110451514-G-T

http://identifiers.org/hco/11/GRCh38#10559397-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#110451670-C-A

10559411-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110451684-G-T

10559642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110451899-G-A

10559642-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110451899-G-T

http://identifiers.org/hco/11/GRCh38#10559751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#110451971-C-A

10559763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110451983-A-G

10560049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110452294-T-C

10560664-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 110453070-T-A

10560664-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 110453070-T-G

10560676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 110453082-A-G

http://identifiers.org/hco/11/GRCh38#10560709-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#110453115-A-C

http://identifiers.org/hco/11/GRCh38#10560717-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#110453123-C-A

10560879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110453252-T-C

10561066-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110453456-T-G

10561294-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110453685-C-G

10561427-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110453821-A-T

10561442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110453828-C-T

10561499-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110453877-A-T

10561709-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110454056-C-G

10561726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110454069-A-G

10561799-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110454142-A-T

10562389-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110457298-G-C

10562525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110457418-C-T

10562570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110457466-C-T

10562771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110457656-C-T

10563688-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110458331-G-C

10563747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110458391-A-G

http://identifiers.org/hco/11/GRCh38#10563892-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#110458518-A-C

10563893-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110458519-G-C

10564102-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110458726-T-A

10564107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110458731-A-G

10564198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110458792-C-T

10564286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110458880-C-T

http://identifiers.org/hco/11/GRCh38#10564340-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#110458934-C-A

10564340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110458934-C-T

http://identifiers.org/hco/11/GRCh38#10564414-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#110459004-C-A

10564414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110459004-C-T

10564746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110459297-G-T

10564902-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110459436-C-G

10565064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110459590-C-T

10565503-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110459988-T-G

10566838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110460282-T-C

10567002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110460431-A-G

10567064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110460448-A-G

10567111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110460494-C-T

10567145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110460552-G-A

10567220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110460625-T-C

10567456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110461177-T-C

10567667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110461392-T-C

http://identifiers.org/hco/11/GRCh38#10568217-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#110461754-A-C

10568327-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110461862-A-T

http://identifiers.org/hco/11/GRCh38#10568328-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#110461863-C-A

10568328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110461863-C-T

http://identifiers.org/hco/11/GRCh38#10568337-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#110461872-C-A

10568337-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110461872-C-G

10568337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110461872-C-T

http://identifiers.org/hco/11/GRCh38#10568341-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#110461876-C-A

10568341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110461876-C-T

http://identifiers.org/hco/11/GRCh38#10568362-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#110461894-C-A

http://identifiers.org/hco/11/GRCh38#10568377-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#110461909-C-A

10568377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110461909-C-T

http://identifiers.org/hco/11/GRCh38#10568384-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#110461916-C-A

10568499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110462042-T-C

10568547-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110462090-C-G

10568584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110462118-A-G

http://identifiers.org/hco/11/GRCh38#10568754-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#110462249-C-A

http://identifiers.org/hco/11/GRCh38#10568858-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#110462353-C-A

10568858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110462353-C-T

http://identifiers.org/hco/11/GRCh38#10573178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#110467570-C-A

10573367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110467741-G-A

10573367-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110467741-G-T

10573516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110467881-A-G

10573520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110467885-G-A

10573559-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110467928-A-T

http://identifiers.org/hco/11/GRCh38#10573611-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#110467967-A-C

10573611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110467967-A-G

10573675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110468025-G-A

10573675-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110468025-G-C

10573675-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110468025-G-T

10573749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110468096-T-C

10573803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110468156-A-G

10573880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110468238-T-C

10573920-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110468277-G-T

10573971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110468326-T-C

http://identifiers.org/hco/11/GRCh38#10574065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#110468403-C-A

10574065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110468403-C-T

http://identifiers.org/hco/11/GRCh38#10574191-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#110468544-C-A

10574191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110468544-C-T

10574384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110468745-G-A

10574475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110468824-T-C

10574588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110468931-G-T

10574630-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110468972-T-G

http://identifiers.org/hco/11/GRCh38#10574884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#110469275-C-A

http://identifiers.org/hco/11/GRCh38#10575493-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#110469799-C-A

10575563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110469873-G-T

10575914-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110470191-A-T

10575928-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110470205-A-T

http://identifiers.org/hco/11/GRCh38#10575937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#110470214-C-A

10575937-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110470214-C-G

10575937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110470214-C-T

10575949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110470226-A-G

10575949-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110470226-A-T

http://identifiers.org/hco/11/GRCh38#10576048-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#110470285-C-A

10576100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110470335-G-A

10576100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110470335-G-T

10576109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110470344-A-G

http://identifiers.org/hco/11/GRCh38#10576118-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#110470353-A-C

10576322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110470556-G-A

10576322-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110470556-G-T

10576326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110470560-G-A

10576422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110470656-A-G

10576603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110470834-C-T

10576604-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110470835-T-G

http://identifiers.org/hco/11/GRCh38#10576660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#110470893-C-A

10576722-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110470955-A-T

10577283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110471091-C-T

10577721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110471487-C-T

10577876-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110471681-C-G

10577950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110471759-C-T

10577978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110471784-T-C

10578198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110472202-T-C

10578223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110472222-G-A

10578252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110472251-G-A

10578252-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110472251-G-T

10578302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110472306-G-A

10578324-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110472332-T-A

10578468-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110472462-G-C

10578498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110472491-G-A

10578637-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110473927-T-A

10578644-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110473934-G-C

10579176-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110474723-C-G

10579459-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110475014-T-G

10579500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110475055-C-T

http://identifiers.org/hco/11/GRCh38#10580140-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#110475756-C-A

10580437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110476028-C-T

10580475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110476066-C-T

10580511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110476102-A-G

10580535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110476126-C-T

10580659-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110476258-G-T

10580671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110476270-G-A

10580671-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110476270-G-T

10580724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110476320-A-G

10580745-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110476341-C-G

http://identifiers.org/hco/11/GRCh38#10580822-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#110476417-C-A

10580822-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110476417-C-G

10581034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110476603-A-G

10581042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110476611-C-T

10581149-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110476683-G-T

10581174-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110476709-T-G

10581543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110477067-C-T

10581616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110477137-T-C

10581618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110477139-G-A

http://identifiers.org/hco/11/GRCh38#10581867-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#110477349-C-A

10581867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 110477349-C-T

10581951-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110477433-G-T

10582029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110477511-G-A

10582029-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110477511-G-C

10582029-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110477511-G-T

10582566-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110478004-G-C

10583358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110478405-G-A

10583434-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110478462-G-C

10583510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110478529-C-T

10583623-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110478621-G-C

10583856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110478816-G-A

http://identifiers.org/hco/11/GRCh38#10583893-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#110478852-A-C

10583955-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110478926-T-G

10584068-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110479041-G-T

http://identifiers.org/hco/11/GRCh38#10584354-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#110479314-C-A

10584649-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110479583-A-T

10584659-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110479593-A-T

10586143-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110480552-G-T

10586174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110480571-T-C

10586174-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110480571-T-G

10586181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110480578-G-A

10586181-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110480578-G-C

10586181-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110480578-G-T

10586183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110480580-G-A

10586183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110480580-G-T

10586215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110480591-T-C

10586216-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110480592-G-C

10586216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110480592-G-T

10586246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110480623-G-A

10586246-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110480623-G-T

10586340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110480717-C-T

http://identifiers.org/hco/11/GRCh38#10586389-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#110480765-A-C

10586389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110480765-A-G

10586865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110480901-G-A

10587050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110481073-C-T

10587110-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110481122-C-G

10587118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110481128-T-C

10587148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110481157-G-A

10587189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110481168-C-T

10587319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110481273-C-T

10587453-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110481414-A-T

10587712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110481631-G-A

10587753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110481669-C-T

10587977-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110481862-C-G

10588813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110482550-A-G

10588916-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110482645-C-G

10588916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110482645-C-T

10588931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110482660-T-C

10589156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110482847-T-C

10589223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110482909-C-T

10589325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110482999-C-T

10589415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110483087-A-G

10589710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110483257-G-A

10589710-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110483257-G-C

10589746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110483307-C-T

10589883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110483425-A-G

10589925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110483468-G-A

10589973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110483505-A-G

10589977-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110483509-T-G

10589983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110483515-G-A

10590239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110483741-G-A

10590306-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110483803-T-A

10590737-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110484233-T-A

10590803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110484288-T-C

10591098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110484459-G-A

10591458-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110484874-T-G

10591677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110485065-G-A

10591677-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110485065-G-T

10591683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110485071-C-T

10591690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110485078-T-C

10591746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110485118-T-C

10591747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110485119-T-C

10591898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110485166-G-A

10591979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110485231-C-T

10592049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110485297-G-A

10592184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110485402-G-A

http://identifiers.org/hco/11/GRCh38#10592327-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#110485647-A-C

10592467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110485867-C-T

10592650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110486067-G-A

10592796-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110486204-C-G

10592809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110486217-T-C

10592880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110486589-G-A

10592913-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110486622-G-T

http://identifiers.org/hco/11/GRCh38#10592946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#110486653-C-A

10593090-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110486801-G-T

10593129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110486835-G-T

http://identifiers.org/hco/11/GRCh38#10593211-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#110486900-A-C

10593241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 110486929-A-G

10593241-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 110486929-A-T

http://identifiers.org/hco/11/GRCh38#10593303-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#110486989-C-A

10593303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 110486989-C-T

http://identifiers.org/hco/11/GRCh38#10593369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#110487047-C-A

http://identifiers.org/hco/11/GRCh38#10593379-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#110487057-C-A

10593379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 110487057-C-T

10593383-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 110487061-T-A

10593383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 110487061-T-C

10593408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 110487086-G-T

http://identifiers.org/hco/11/GRCh38#10593412-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#110487090-C-A

10593529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 110487185-G-A

10593614-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 110487270-G-T

10593615-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 110487271-T-A

10593615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 110487271-T-C

10593616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 110487272-G-A

10593616-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 110487272-G-T

10593654-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 110487311-T-G

http://identifiers.org/hco/11/GRCh38#10593673-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#110487329-A-C

10593673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 110487329-A-G

10593687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 110487343-T-C

http://identifiers.org/hco/11/GRCh38#10593725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#110487370-C-A

10593725-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 110487370-C-G

10593725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 110487370-C-T

10593727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 110487372-G-A

10593727-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 110487372-G-T

10593729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 110487374-A-G

10593753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 110487402-A-G

10593756-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 110487405-G-C

10593881-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 110487496-A-T

http://identifiers.org/hco/11/GRCh38#10593895-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#110487510-C-A

10593896-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 110487511-T-A

10593896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 110487511-T-C

http://identifiers.org/hco/11/GRCh38#10593986-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#110487598-A-C

10593992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 110487604-G-A

http://identifiers.org/hco/11/GRCh38#10594026-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#110487633-A-C

10594026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110487633-A-G

http://identifiers.org/hco/11/GRCh38#10594367-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#110487972-C-A

10594367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110487972-C-T

10594527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110488124-C-T

10594727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110488318-G-A

10594978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110488474-G-A

10595188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110488572-G-A

10595188-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110488572-G-C

10595188-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110488572-G-T

10595433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110488788-T-C

10595537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110488950-T-C

http://identifiers.org/hco/11/GRCh38#10599669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#110493376-C-A

10599669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110493376-C-T

http://identifiers.org/hco/11/GRCh38#10599750-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#110493457-C-A

10599750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 110493457-C-T

10599787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43434
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 110493495-G-T