213818697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190076350-G-A

213818697-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190076350-G-T

213818778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190076269-G-A

http://identifiers.org/hco/1/GRCh38#213818812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190076238-C-A

213818918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190076134-T-C

http://identifiers.org/hco/1/GRCh38#213818937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190076117-C-A

213818937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190076117-C-T

213819014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190076050-C-T

http://identifiers.org/hco/1/GRCh38#213819071-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190075993-C-A

213819098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190075966-A-G

http://identifiers.org/hco/1/GRCh38#213819099-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190075965-C-A

213819552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190075518-G-A

213819552-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190075518-G-T

213819595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190075466-C-T

213819605-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190075456-G-C

213819702-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190075372-G-T

213819943-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190075156-G-T

213820131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190074999-T-C

213820266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190074878-A-G

213820267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190074877-G-T

213820268-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190074876-G-C

213820269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190074875-A-G

http://identifiers.org/hco/1/GRCh38#213820277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190074859-C-A

213820309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190074827-C-T

213820596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190074230-T-C

213820680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190074167-A-G

213820701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190074146-G-T

213820768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190074071-G-A

213820768-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190074071-G-T

http://identifiers.org/hco/1/GRCh38#213820781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190074058-C-A

213820885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190073965-A-G

213821054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190073554-A-G

213821080-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190073532-G-T

http://identifiers.org/hco/1/GRCh38#213821111-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190073501-C-A

213821111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190073501-C-T

213821145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190073480-C-T

213821157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190073468-G-T

213821173-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190073452-T-A

213821173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190073452-T-C

http://identifiers.org/hco/1/GRCh38#213821198-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190073427-C-A

213821198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190073427-C-T

213821219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190073405-G-A

213821219-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190073405-G-T

213821238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190073388-G-A

213821238-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190073388-G-T

http://identifiers.org/hco/1/GRCh38#213821361-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190073294-C-A

213821361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190073294-C-T

213821539-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190073139-C-G

213821554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190073125-G-T

http://identifiers.org/hco/1/GRCh38#213821604-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190073097-C-A

http://identifiers.org/hco/1/GRCh38#213821654-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190073046-C-A

213821654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190073046-C-T

http://identifiers.org/hco/1/GRCh38#213821660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190073040-C-A

213821660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190073040-C-T

http://identifiers.org/hco/1/GRCh38#213821703-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190073017-A-C

213821703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190073017-A-G

213821806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190072923-A-G

213821810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190072919-G-A

213821846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190072883-G-A

213821846-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190072883-G-T

213821855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190072874-G-A

213821855-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190072874-G-T

http://identifiers.org/hco/1/GRCh38#213821893-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190072845-C-A

213821903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190072839-T-C

213821922-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190072820-G-T

213821949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190072795-T-C

213821949-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190072795-T-G

213822020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190072738-G-A

213822020-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190072738-G-T

213822040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190072718-T-C

http://identifiers.org/hco/1/GRCh38#213822091-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190072672-A-C

213822186-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190072612-G-T

213822258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190072555-G-A

213822452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190072378-A-G

213822509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190072318-C-T

http://identifiers.org/hco/1/GRCh38#213822535-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190072292-C-A

213825079-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190072016-G-C

213825116-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190071979-T-C

213825137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190071959-A-G

213825391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190071723-A-G

213825519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190071597-A-G

213825552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190071564-C-T

213825679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190071439-C-T

213825711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190071406-A-G

213825766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190071355-T-C

http://identifiers.org/hco/1/GRCh38#213825896-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190071187-A-C

213826144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190070945-G-A

213826212-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190070884-G-C

213826212-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190070884-G-T

213826238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190070857-A-G

213826256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190070839-G-A

213826471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190070666-T-C

213826615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190070523-T-C

213826928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190070216-A-G

213827090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190070077-G-A

213827090-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190070077-G-T

213827642-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190069543-A-T

213827711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190069483-G-A

213827855-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190069352-T-G

213828115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190069118-A-G

213828329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190068923-C-T

213828330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190068922-C-T

213828345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190068907-G-A

213828345-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190068907-G-C

213828597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190068654-T-C

213828612-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190068639-G-C

213828615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190068636-A-G

213828917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190067840-C-T

213828920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190067837-A-G

213829149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190067600-T-C

213829223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190067526-T-C

213829357-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190067409-G-C

213829478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190066986-G-A

213829558-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190066906-T-A

213829602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190066862-A-G

213829621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190066848-C-T

213830296-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190066161-A-T

213830520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190065916-C-T

213830643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190065808-A-G

213830643-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190065808-A-T

http://identifiers.org/hco/1/GRCh38#213830692-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190065770-C-A

213830830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190065626-C-T

213830850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190065606-G-A

213831223-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190065245-T-G

213831261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190065207-A-G

213831308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190065161-C-T

213831470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190065017-T-C

http://identifiers.org/hco/1/GRCh38#213831527-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190064961-C-A

http://identifiers.org/hco/1/GRCh38#213831666-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190064836-A-C

213837254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190062409-G-A

213837651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190062017-T-C

213837726-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190061949-C-G

213837904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190061785-A-G

213838091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190061640-T-C

213838485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190061497-G-A

213838632-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190061376-T-G

213838649-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190061359-C-G

213838823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190061187-G-A

213838861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190061151-T-C

http://identifiers.org/hco/1/GRCh38#213840444-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190060348-C-A

213840444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190060348-C-T

213840476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190060317-A-G

213840493-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190060302-T-A

213840493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190060302-T-C

213840493-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190060302-T-G

213840844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190059965-A-G

http://identifiers.org/hco/1/GRCh38#213840877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190059935-C-A

213840877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190059935-C-T

http://identifiers.org/hco/1/GRCh38#213840920-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190059893-C-A

213840920-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190059893-C-G

213840960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190059851-G-A

213840960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190059851-G-T

http://identifiers.org/hco/1/GRCh38#213841278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190059602-C-A

213841319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190059561-G-A

213841330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190059546-T-C

213841357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190059519-G-A

213841602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190059282-C-T

213841939-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190058966-A-G

213841950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190058955-G-A

213841950-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190058955-G-T

213841969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190058927-T-C

213842066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190058845-T-C

http://identifiers.org/hco/1/GRCh38#213842175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190058769-C-A

213842175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190058769-C-T

213842176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190058768-G-A

213842253-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190058698-A-T

213842280-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190058673-A-T

213842299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190058656-T-C

213842367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190058590-C-T

http://identifiers.org/hco/1/GRCh38#213842377-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190058580-C-A

213842410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190058550-T-C

213842869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190058010-T-C

213842872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190058007-T-C

213842978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190057216-T-C

213842978-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190057216-T-G

http://identifiers.org/hco/1/GRCh38#213843146-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190057032-A-C

213843225-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190056981-T-A

213843403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190056827-G-A

213843403-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190056827-G-T

213843482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 190056757-C-T

213843521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190056718-C-T

http://identifiers.org/hco/1/GRCh38#213843525-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190056715-C-A

213844207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190055972-T-C

213844664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190055473-G-A

213845402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190054144-A-G

213845678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190053899-G-A

213845830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190053751-A-G

213845896-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190053703-G-C

213845944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190053657-C-T

213846953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190052758-A-G

213847051-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190052657-G-C

http://identifiers.org/hco/1/GRCh38#213847285-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190052460-C-A

213847293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190052452-G-T

213847471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190052281-C-T

http://identifiers.org/hco/1/GRCh38#213847654-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190052158-C-A

213847745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190052081-A-G

213847780-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190052053-T-G

213848028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190051868-T-C

213848035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190051861-T-C

213848900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190048889-G-A

213848959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190048855-A-G

213849083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190048765-G-A

http://identifiers.org/hco/1/GRCh38#213849116-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190048735-A-C

213849116-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190048735-A-T

213849211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190048599-T-C

213849617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190048055-G-A

http://identifiers.org/hco/1/GRCh38#213849717-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190047954-C-A

213849898-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190047774-G-T

213850367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190047326-T-C

213850387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190047306-C-T

213851840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190045749-C-T

213851908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190045705-T-C

213851915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190045699-C-T

213851954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190045661-C-T

213852184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190045453-G-A

http://identifiers.org/hco/1/GRCh38#213853450-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190043977-A-C

213853479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190043948-A-G

213853522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190043895-C-T

http://identifiers.org/hco/1/GRCh38#213853593-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190043833-A-C

213853781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190043672-G-A

213853951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190043512-G-A

213854130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190043348-A-G

213854140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190043315-G-A

213854145-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190043310-C-G

213854145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190043310-C-T

213854212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190043254-T-C

213857739-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190040083-C-G

213857761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190040060-C-T

213858366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190039240-C-T

213858804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190038781-G-A

213859002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190038598-A-G

213859011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190038589-C-T

213859235-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190038368-G-T

213859426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190038029-C-T

http://identifiers.org/hco/1/GRCh38#213859661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190037804-C-A

213859699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190037777-C-T

213859777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190037712-G-A

213859886-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190037611-A-G

213859890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190037607-A-G

213859917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190037580-C-T

http://identifiers.org/hco/1/GRCh38#213859971-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190037528-C-A

213860037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190037462-G-A

http://identifiers.org/hco/1/GRCh38#213860085-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190037423-A-C

213860085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190037423-A-G

213860100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190037417-T-C

213860130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190037393-T-C

213860179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190037385-A-G

213860318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190037233-G-A

213860318-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190037233-G-C

213860596-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190037003-C-G

213860596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190037003-C-T

213860643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190036965-A-G

213862497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190032118-C-T

213862526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190032097-C-T

213862571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190032056-C-T

213862591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190032036-G-A

213862597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190032028-A-G

213862612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190032013-A-G

213862622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190031997-C-T

213862672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190031946-A-G

213862807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190031784-G-A

213863802-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190030820-C-G

213863892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190030728-T-C

213864610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190030061-C-T

213864623-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190030048-C-G

213864789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190029909-G-A

213864852-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190029835-T-G

213865041-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190029684-T-A

213865082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190029652-T-C

213866285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190029056-C-T

213866334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190029002-G-A

http://identifiers.org/hco/1/GRCh38#213866359-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190028983-A-C

213866424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190028868-A-G

213866469-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190028835-G-C

213866747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190028591-T-C

213867006-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190028351-C-G

http://identifiers.org/hco/1/GRCh38#213867114-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190028236-A-C

213867114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190028236-A-G

213867128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190028222-G-A

213867130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190028220-G-A

213867130-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190028220-G-C

213867342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190028055-T-C

213867349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190028048-A-G

213867532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190027865-C-T

213867588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190027809-T-C

213867755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190027661-A-G

213867959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190027458-G-A

213868011-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190027414-T-G

213868013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190027412-G-A

213868047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190027373-C-T

213868082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190027338-A-G

213868191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190027262-G-A

213868393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190027051-C-T

http://identifiers.org/hco/1/GRCh38#213869788-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190024447-C-A

http://identifiers.org/hco/1/GRCh38#213870243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190023619-C-A

213870243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190023619-C-T

213870329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190023532-G-A

213870399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190023475-C-T

213870507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190023384-G-T

213870729-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190023167-T-A

213870809-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190023087-G-T

213870832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190023064-T-C

213870851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190023052-A-G

http://identifiers.org/hco/1/GRCh38#213870879-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190023024-C-A

213870887-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190023016-G-T

213871023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190022896-T-C

213871363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190022551-C-T

213876127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190020290-G-A

http://identifiers.org/hco/1/GRCh38#213876185-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190020223-C-A

http://identifiers.org/hco/1/GRCh38#213876337-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190020070-C-A

213876435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190019978-C-T

213876557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190019887-T-C

http://identifiers.org/hco/1/GRCh38#213876607-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190019836-C-A

213876607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190019836-C-T

213876768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190019300-A-G

http://identifiers.org/hco/1/GRCh38#213876800-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190019268-C-A

213876903-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190019158-G-T

213877156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190018907-A-G

213877700-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190018372-A-T

213877724-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190018361-A-T

213878354-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190017764-C-G

213878414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190017708-A-G

213878549-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190017554-T-G

http://identifiers.org/hco/1/GRCh38#213879096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190017003-C-A

http://identifiers.org/hco/1/GRCh38#213879201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190016895-C-A

213879201-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190016895-C-G

213882418-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190015534-T-C

213882448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190015504-C-T

213882543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190015418-G-A

213882648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190015308-G-A

213882728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190015252-C-T

213883829-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190013591-G-C

213883916-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190013506-A-T

213884272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190013164-C-T

213884426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190013013-C-T

213885395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190012171-T-C

213885402-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190012164-A-T

213885515-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190012060-G-C

213887010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190009091-G-A

213887010-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190009091-G-C

http://identifiers.org/hco/1/GRCh38#213887096-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190009013-A-C

213887096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190009013-A-G

213887160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190008955-G-A

213887211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190008902-A-G

213887355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190008802-A-G

213887499-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190008645-T-G

http://identifiers.org/hco/1/GRCh38#213887566-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190008586-C-A

213887566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190008586-C-T

213887689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190008462-T-C

213887833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190008356-A-G

213887891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190008299-T-C

213887891-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190008299-T-G

213888018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190008170-G-A

213888020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190008168-G-A

213888174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190007855-G-A

http://identifiers.org/hco/1/GRCh38#213888259-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190007773-C-A

213888259-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190007773-C-G

213888259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190007773-C-T

213888304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190007701-T-C

213888432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190007565-A-G

http://identifiers.org/hco/1/GRCh38#213888441-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190007550-C-A

213888494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190007495-T-C

213888509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190007483-T-C

213888517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190007475-G-A

http://identifiers.org/hco/1/GRCh38#213888528-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190007464-C-A

213888528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190007464-C-T

213888769-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190007246-C-G

213888822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190007206-T-C

213889510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190006168-T-C

213889892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190005589-A-G

213889946-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190005533-T-G

213889968-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190005511-C-G

213890109-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190005350-C-G

213890446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190004972-T-C

http://identifiers.org/hco/1/GRCh38#213890478-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190004941-A-C

213890478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190004941-A-G

213890562-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190004854-G-T

213890695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190004717-C-T

213891688-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190003635-G-C

213891767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190003567-T-C

213892086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190003397-A-G

213892094-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190003389-T-G

213892214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190003313-G-A

213892216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190003311-G-A

213892290-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190003239-A-G

213892907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190002647-G-A

213892941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190002615-A-G

213893124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190002441-A-G

213893193-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190002372-G-C

213893193-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190002372-G-T

213894127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190001799-T-C

http://identifiers.org/hco/1/GRCh38#213894128-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190001798-C-A

http://identifiers.org/hco/1/GRCh38#213894313-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190001628-C-A

http://identifiers.org/hco/1/GRCh38#213894436-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190001540-C-A

213894436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190001540-C-T

213894737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190001291-G-A

213894781-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190001255-G-T

213894848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190001202-T-C

213895001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190001079-C-T

213895234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190000757-G-A

213895302-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190000690-T-A

http://identifiers.org/hco/1/GRCh38#213895573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190000429-C-A

213895573-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190000429-C-G

213896030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190000027-G-A

213896030-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190000027-G-T

213896046-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190000012-A-T

213896072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189999988-G-A

213896072-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189999988-G-T

213896164-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189999908-G-C

213896262-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189999815-C-G

213896262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189999815-C-T

213896353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189999720-T-C

213896361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189999712-C-T

213896917-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189999207-T-G

213896959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189999172-T-C

213898179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189998728-C-T

213898466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189998439-G-A

213898467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189998438-G-A

213899160-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189997348-T-A

213899160-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189997348-T-G

213899298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189997211-A-G

213899438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189997104-A-G

http://identifiers.org/hco/1/GRCh38#213900015-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189996532-A-C

213900037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189996512-G-A

213900891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189996167-G-A

213901033-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189996047-C-G

http://identifiers.org/hco/1/GRCh38#213901290-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189995590-C-A

http://identifiers.org/hco/1/GRCh38#213901345-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189995528-C-A

213901345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189995528-C-T

213901359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189995514-T-C

http://identifiers.org/hco/1/GRCh38#213901414-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189995459-A-C

213901587-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189995293-G-T

http://identifiers.org/hco/1/GRCh38#213902656-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189994672-A-C

213902690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189994644-A-G

213902740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189994588-T-C

213903420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189994024-C-T

213903424-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189994020-G-C

213903474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189993990-G-T

213903476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189993988-A-G

213903621-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189993850-G-C

213903761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189993703-G-A

213904538-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189992906-T-G

213904724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189992706-A-G

213904787-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189992642-G-C

213904904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189992564-A-G

213904905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189992563-G-A

http://identifiers.org/hco/1/GRCh38#213904906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189992562-C-A

213905118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189992367-G-A

213905118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189992367-G-T

213905227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189992280-G-A

213905464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189992082-G-A

213905464-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189992082-G-T

213905726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189991826-G-A

213905741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189991811-T-C

213905814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189991739-C-T

213905823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189991730-G-A

213905852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189991705-C-T

213905860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189991697-T-C

213905914-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189991636-A-T

213906311-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189990866-T-G

213906335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189990845-C-T

213906427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189990767-C-T

213906615-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189990639-T-G

213906733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189990532-C-T

213906785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189990500-A-G

213906829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189990456-A-G

213906860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189990435-A-G

213906865-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189990432-G-C

213907010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189989789-A-G

213907170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189989670-G-A

213907175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189989665-G-A

213907195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189989637-G-A

213907469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189989395-T-C

213907611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189989260-A-G

213907703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189989172-G-A

213908071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189988949-G-A

213908269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189988788-A-G

213908504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189988587-A-G

213909051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189986837-G-A

213909066-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189986822-A-T

213909084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189986805-A-G

http://identifiers.org/hco/1/GRCh38#213909121-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189986769-A-C

213909230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189986667-G-A

http://identifiers.org/hco/1/GRCh38#213909317-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189986579-A-C

213909355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189986541-G-A

http://identifiers.org/hco/1/GRCh38#213909403-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189986493-C-A

213909403-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189986493-C-G

213909403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189986493-C-T

213910138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189985784-G-A

213910171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189985753-G-A

213910241-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189985692-G-T

213910273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189985660-A-G

http://identifiers.org/hco/1/GRCh38#213910507-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189985596-A-C

213910518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189985585-A-G

213910538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189985565-C-T

213910920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189985395-A-G

213910996-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189985321-C-G

213911004-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189985312-G-C

213911008-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189985308-A-T

213911202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189985034-G-A

213911437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189984769-T-C

213911570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189984666-C-T

213911632-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189984615-T-G

213914208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189983338-T-C

213914498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189983040-C-T

http://identifiers.org/hco/1/GRCh38#213914512-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189983026-C-A

213914661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189982879-G-A

213914706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189982828-T-C

213914797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189982625-G-A

213914797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189982625-G-T

213914798-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189982624-T-A

213914798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189982624-T-C

213914851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189982571-C-T

213914877-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189982552-T-A

213914968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189982357-G-T

http://identifiers.org/hco/1/GRCh38#213914996-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189982318-A-C

http://identifiers.org/hco/1/GRCh38#213915055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189982163-C-A

213915165-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189982051-C-G

213915208-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189982020-G-C

http://identifiers.org/hco/1/GRCh38#213915212-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189982016-C-A

213915238-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189981990-G-T

213917193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189977671-C-T

213917238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189977628-C-T

213917460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189977453-G-A

http://identifiers.org/hco/1/GRCh38#213918386-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189977181-C-A

213918643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189976942-G-T

213918654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189976931-T-C

213918826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189976784-A-G

213918918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189976712-C-T

213918995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189976635-G-A

213919024-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189976620-T-A

213920817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189975788-T-C

http://identifiers.org/hco/1/GRCh38#213920873-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189975729-C-A

213920873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189975729-C-T

213921553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189974914-C-T

213922517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189973688-A-G

213922832-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189973433-T-A

213925084-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189973385-C-G

213925087-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189973382-T-C

213925107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189973362-T-C

213925221-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189973254-T-A

213925234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189973242-T-C

213925299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189973188-G-A

213925412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189973080-A-G

213925552-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189972763-G-T

213925848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189972451-A-G

213925992-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189972311-G-T

213926136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189972172-T-C

213926314-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189972005-G-C

213926314-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189972005-G-T

http://identifiers.org/hco/1/GRCh38#213926338-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189971981-A-C

213926500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189971831-G-A

213926500-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189971831-G-T

213926535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189971796-A-G

213926553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189971782-A-G

http://identifiers.org/hco/1/GRCh38#213926662-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189971698-C-A

213926662-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189971698-C-G

213926662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189971698-C-T

213926671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189971689-A-G

213926671-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189971689-A-T

213926743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189971631-T-C

http://identifiers.org/hco/1/GRCh38#213926760-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189971607-A-C

http://identifiers.org/hco/1/GRCh38#213926816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189971557-C-A

213926863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189971510-T-C

213927392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189971051-C-T

213927614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189970882-C-T

213927718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189970788-C-T

213927779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189970728-A-G

213927796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189970711-C-T

213927867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189970633-C-T

213927932-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189970567-C-G

213927932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189970567-C-T

213928143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189970362-G-A

213928172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189970334-G-A

http://identifiers.org/hco/1/GRCh38#213928286-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189970228-C-A

213928286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189970228-C-T

http://identifiers.org/hco/1/GRCh38#213928375-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189970134-A-C

213928590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189969918-C-T

213928871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189969650-G-A

213928883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189969639-G-A

213928928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189969604-T-C

http://identifiers.org/hco/1/GRCh38#213928966-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189969568-C-A

213928966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189969568-C-T

213929141-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189969416-G-C

213929205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189969364-G-A

213929280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189969310-G-A

213929351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189969243-A-G

213929393-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189969204-T-G

213929564-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189969034-T-A

http://identifiers.org/hco/1/GRCh38#213929610-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189968988-A-C

http://identifiers.org/hco/1/GRCh38#213929666-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189968932-A-C

http://identifiers.org/hco/1/GRCh38#213929753-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189968844-C-A

213930001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189968640-C-T

213930073-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189968560-T-A

213930073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189968560-T-C

213930576-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189966753-G-T

213930633-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189966326-C-G

http://identifiers.org/hco/1/GRCh38#213930637-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189966322-C-A

213930789-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189966184-G-T

213930858-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189966114-C-G

213930921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189966061-C-T

213931025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189965976-A-G

http://identifiers.org/hco/1/GRCh38#213931035-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189965966-C-A

213931040-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189965961-G-C

http://identifiers.org/hco/1/GRCh38#213931521-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189965514-A-C

213931575-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189965463-G-T

213931756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189964930-G-A

http://identifiers.org/hco/1/GRCh38#213931946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189964744-C-A

213931971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189964718-C-T

213932045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 189964657-G-A

213932045-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 189964657-G-T

213932195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189964502-G-A

213932332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189964371-C-T

213932361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189964342-T-C

213932515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189964181-G-A

213932620-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189964066-C-G

213933084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189963650-A-G

213933876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189962899-C-T

213933992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189962340-A-G

213934052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189962280-T-C

213934361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189962012-G-A

213934361-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189962012-G-C

213934361-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189962012-G-T

213934365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189962008-G-A

213934738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189961698-T-C

213934878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189961564-G-T

213935186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189961276-T-C

213935353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189961117-G-A

213940849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-C

213940868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

213941520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189953409-A-G

http://identifiers.org/hco/1/GRCh38#213941653-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189953279-A-C

213941690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189953251-G-A

http://identifiers.org/hco/1/GRCh38#213941807-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189953147-A-C

213941807-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189953147-A-T

213942028-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189952989-T-G

213942085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189952945-G-A

213942576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189952457-A-G

213942601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189952434-G-A

213942701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189951800-A-G

213942703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189951798-G-A

213943373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189951054-G-A

213943394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189951033-G-A

213943420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189951007-A-G

213944149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189950391-C-T

213944326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189949553-T-C

213944613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189949313-C-T

213944621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189949305-T-C

http://identifiers.org/hco/1/GRCh38#213944681-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189949263-C-A

213944748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189949196-A-G

213944881-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189949081-G-T

213944888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189949074-A-G

213944942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189949020-T-C

213944969-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189948993-C-G

213945143-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189948824-G-C

213945419-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189948560-T-A

213945421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189948558-T-C

213946496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189948076-G-A

213946627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189947947-C-T

http://identifiers.org/hco/1/GRCh38#213946744-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189947831-A-C

213946884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189947453-T-C

213946910-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189947428-T-G

213946947-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189947391-T-A

213947144-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189947223-A-T

213947283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189947084-C-T

http://identifiers.org/hco/1/GRCh38#213947290-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189947077-C-A

213947290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189947077-C-T

213947652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189946704-G-A

213947670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189946686-T-C

213947699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189946656-G-A

213948046-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189946197-G-T

213948100-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189946135-G-C

213948105-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189946130-T-A

213948127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189946107-A-G

213948376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189945934-A-G

http://identifiers.org/hco/1/GRCh38#213948503-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189945810-C-A

213948588-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189945717-T-A

213948588-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189945717-T-G

213948634-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189945671-A-G

213948790-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189945512-T-G

213949377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189943637-T-C

http://identifiers.org/hco/1/GRCh38#213949524-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189943486-C-A

213949524-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189943486-C-G

213949537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189943473-T-C

213949653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189943389-G-A

213949657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189943385-T-C

213949663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189943379-G-A

213949664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189943378-C-T

http://identifiers.org/hco/1/GRCh38#213949711-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189943337-A-C

213949897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189943134-A-G

213950320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189942661-G-A

213950320-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189942661-G-T

213950330-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189942648-T-A

213950755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189942228-G-A

213951244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189941760-T-C

213951259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189941745-C-T

213951558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189941182-T-C

213951853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189941009-C-T

http://identifiers.org/hco/1/GRCh38#213952027-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189940839-A-C

http://identifiers.org/hco/1/GRCh38#213952140-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189940735-A-C

213952193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189940684-A-G

213952209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189940668-T-C

213952250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189940627-C-T

213952511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189940424-A-G

213952511-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189940424-A-T

http://identifiers.org/hco/1/GRCh38#213952540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189940396-C-A

213952540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189940396-C-T

213952547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189940389-C-T

213952830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189940184-A-G

213953018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189939994-G-A

213953341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189939919-C-T

213953608-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189939689-C-G

213953780-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189939535-G-T

213953921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189939396-G-A

213954359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189938922-C-T

213954459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189938742-T-C

213954512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189938669-C-T

213954522-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189938659-T-G

213954523-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189938658-A-T

213955342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189938405-G-A

213955344-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189938403-G-C

213955346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189938401-T-C

213955346-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189938401-T-G

213955393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189938360-T-C

213955437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189938319-G-A

213955943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189937497-T-C

213956049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189937414-C-T

213956069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189937394-T-C

213956093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189937371-G-A

213956093-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189937371-G-C

213956101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189937362-T-C

213956286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189937178-C-T

213956293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189937171-G-A

213956788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189936667-T-C

213957298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189936144-G-A

213957298-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189936144-G-C

213957513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189935835-A-G

213957750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189935605-C-T

213957881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189935487-A-G

213957896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189935472-T-C

213958437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 189934238-G-A

213958558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 189934123-C-T

213958909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189933765-A-G

http://identifiers.org/hco/1/GRCh38#213959163-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189933547-C-A

213959163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189933547-C-T

213959296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189933432-T-C

213959356-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189933396-C-G

http://identifiers.org/hco/1/GRCh38#213959424-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189933333-C-A

http://identifiers.org/hco/1/GRCh38#213959588-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189933170-A-C

213960023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189932766-T-C

213960035-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189932756-T-G

213960064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189932732-A-G

213960202-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189932590-G-C

213960238-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189932554-C-G

213960238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189932554-C-T

213960674-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189932227-G-T

http://identifiers.org/hco/1/GRCh38#213960803-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189932115-A-C

213960878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189932040-G-A

http://identifiers.org/hco/1/GRCh38#213961050-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189931956-C-A

213961265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189931781-A-G

213961295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189931751-T-C

213961482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189931569-C-T

213961494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189931557-A-G

213961731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189931069-A-G

213961974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189930866-T-C

213961975-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189930865-A-G

213962004-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189930200-C-G

213962440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189929761-A-G

213962559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189929657-G-T

http://identifiers.org/hco/1/GRCh38#213962719-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189929527-C-A

213962721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189929525-A-G

http://identifiers.org/hco/1/GRCh38#213962838-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189929414-A-C

213963612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189928440-A-G

213963711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189928344-T-C

213963713-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189928342-T-A

213963736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189928106-A-G

http://identifiers.org/hco/1/GRCh38#213963813-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189928028-C-A

213963889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189927984-G-A

http://identifiers.org/hco/1/GRCh38#213964022-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189927887-A-C

213964025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189927884-A-G

213964026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189927883-G-A

213964027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189927882-G-A

213964027-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189927882-G-C

213964027-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189927882-G-T

213965874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189927309-G-A

213966010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189927176-A-G

213966024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189927162-G-A

http://identifiers.org/hco/1/GRCh38#213966113-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189927107-C-A

213966116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189927104-G-A

213966181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189927038-G-A

http://identifiers.org/hco/1/GRCh38#213966220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189927008-C-A

213966223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189927005-A-G

http://identifiers.org/hco/1/GRCh38#213966224-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189927004-C-A

213966307-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189926927-G-T

213966370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189926865-G-A

213966370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189926865-G-T

213967649-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189925319-A-T

213967767-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189925229-T-A

http://identifiers.org/hco/1/GRCh38#213967793-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189925213-A-C

213967796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189925210-A-G

213967808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189925201-G-T

213968003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189925045-A-G

213968173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189924858-C-T

http://identifiers.org/hco/1/GRCh38#213968285-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189924748-C-A

213968305-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189924737-C-G

213968389-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189924651-C-G

213968556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189924484-G-A

213968558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189924482-G-A

213968558-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189924482-G-C

http://identifiers.org/hco/1/GRCh38#213968623-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189924412-C-A

213969406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189923635-T-C

213969922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189923131-C-T

213970020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189923038-G-A

213970170-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189922890-G-T

213970216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189922844-G-A

213970562-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189922449-G-T

213971000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189921612-G-A

213971355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189921302-C-T

213974657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189918501-G-A

http://identifiers.org/hco/1/GRCh38#213975210-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189917787-A-C

http://identifiers.org/hco/1/GRCh38#213975401-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189917602-A-C

213975497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189917518-T-C

213975628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189917385-T-C

http://identifiers.org/hco/1/GRCh38#213975715-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189917303-A-C

213975769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189917247-G-A

213976136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189916927-T-C

http://identifiers.org/hco/1/GRCh38#213976240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189916840-C-A

http://identifiers.org/hco/1/GRCh38#213976244-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189916836-C-A

213976785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189914845-A-G

213977025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189914664-C-T

213977092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189914599-G-T

213977096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189914595-C-T

http://identifiers.org/hco/1/GRCh38#213977113-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#189914570-C-A

http://identifiers.org/hco/1/GRCh38#213977128-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189914555-C-A

213977128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 189914555-C-T

213977147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189914538-G-A

213977147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189914538-G-T

213977202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189914488-G-A

213977202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189914488-G-T

213977292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189914420-G-A

213977292-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189914420-G-T

213977448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189914300-T-C

213977586-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189914149-G-T

213977832-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189913901-G-C

213977890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189913846-G-A

http://identifiers.org/hco/1/GRCh38#213978068-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189913564-A-C

213978068-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189913564-A-T

213978343-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189913224-A-T

213978392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189913175-G-A

213978396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189913171-T-C

213978629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189912936-A-G

213978747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189912837-G-A

213978868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189912693-T-C

213979386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189911114-G-A

213979462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189911036-C-T

213979504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189910995-G-A

213979504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189910995-G-T

http://identifiers.org/hco/1/GRCh38#213979525-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189910974-C-A

http://identifiers.org/hco/1/GRCh38#213979782-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189910725-C-A

213979805-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189910704-T-G

213980007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 189910471-G-A

213980024-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 189910456-G-T

213980050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 189910416-A-G

213980224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189910250-C-T

213980310-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189910152-G-C

http://identifiers.org/hco/1/GRCh38#213980359-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189910083-A-C

213980467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189909885-C-T

http://identifiers.org/hco/1/GRCh38#213980479-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189909873-C-A

213980558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189909794-G-A

213980611-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189909752-A-T

213980655-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189909709-C-G

http://identifiers.org/hco/1/GRCh38#213980990-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189909431-A-C

213981006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189909418-G-A

http://identifiers.org/hco/1/GRCh38#213981146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189909273-C-A

213981268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189909156-A-G

213981268-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189909156-A-T

213981295-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 189909129-C-G

213981358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189909036-T-C

213981369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189909025-T-C

http://identifiers.org/hco/1/GRCh38#213981479-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189908941-C-A

http://identifiers.org/hco/1/GRCh38#213981495-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189908923-C-A

213981495-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189908923-C-G

213981641-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189908730-T-G

213981811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189908586-C-T

213981824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189908573-C-T

http://identifiers.org/hco/1/GRCh38#213982129-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189908324-A-C

213982129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189908324-A-G

213982169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189908281-G-A

213982169-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189908281-G-T

213982677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 189907839-G-A

213982677-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 189907839-G-T

213982921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189907606-G-A

213983062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189907500-C-T

213983065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189907497-T-C

213983065-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189907497-T-G

http://identifiers.org/hco/1/GRCh38#213983180-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#189907411-C-A

213983180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 189907411-C-T

213983188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 189907403-G-A

http://identifiers.org/hco/1/GRCh38#213983214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#189907377-C-A

213983214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 189907377-C-T

213983373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 189907286-G-A

213983373-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 189907286-G-T

http://identifiers.org/hco/1/GRCh38#213983414-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189907252-C-A

http://identifiers.org/hco/1/GRCh38#213983569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189907112-C-A

213983700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189906970-T-C

http://identifiers.org/hco/1/GRCh38#213983736-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189906935-C-A

213983737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189906931-T-C

213983821-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189906835-T-C

213983824-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189906831-G-T

213983877-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189906750-G-T

213983900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189906727-A-G

213983916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189906715-A-G

213983948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189906683-C-T

http://identifiers.org/hco/1/GRCh38#213984088-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189906548-C-A

213984088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189906548-C-T

213984107-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189906529-G-C

http://identifiers.org/hco/1/GRCh38#213984126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189906510-C-A

213984126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189906510-C-T

213984206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189906419-G-A

213984206-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189906419-G-T

213984346-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189906278-A-T

http://identifiers.org/hco/1/GRCh38#213984382-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189906235-C-A

213984495-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189906119-G-T

213984498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189906116-G-A

213984498-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189906116-G-T

213984994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189905662-T-C

213985095-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189905577-G-T

213985217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189905460-G-A

213985217-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189905460-G-T

213985229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189905448-G-A

http://identifiers.org/hco/1/GRCh38#213985827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189904873-C-A

213985827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189904873-C-T

213985994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189904769-G-A

213985994-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189904769-G-T

http://identifiers.org/hco/1/GRCh38#213986120-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189904675-C-A

213986143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189904649-G-A

213986195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189904618-G-A

http://identifiers.org/hco/1/GRCh38#213986246-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189904563-C-A

213986246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189904563-C-T

213986293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189904519-G-A

213986293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189904519-G-T

http://identifiers.org/hco/1/GRCh38#213986301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189904511-C-A

213986301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189904511-C-T

213986331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189904481-T-C

213986899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189903907-T-C

213986926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189903882-A-G

213987279-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189903552-T-A

http://identifiers.org/hco/1/GRCh38#213987355-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189903478-C-A

213987390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189903443-G-T

213987429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 189903398-C-T

http://identifiers.org/hco/1/GRCh38#213987438-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#189903389-A-C

213987527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189903303-G-A

213987527-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189903303-G-C

213987527-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189903303-G-T

213987709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189903141-G-A

213987709-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 189903141-G-C

213988085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 189902788-T-C

213988122-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 189902750-T-A

213988122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 189902750-T-C

213988122-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 189902750-T-G

213988249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 189902689-C-T

http://identifiers.org/hco/1/GRCh38#213988460-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#189902486-C-A

213988460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43656
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 189902486-C-T