http://identifiers.org/hco/12/GRCh38#69825283-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#116732800-C-A

69825283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: 5 prime UTR variant
orthologous variants: 116732800-C-T

69825308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: 5 prime UTR variant
orthologous variants: 116732775-T-C

69825342-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: 5 prime UTR variant
orthologous variants: 116732742-A-T

69825351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: 5 prime UTR variant
orthologous variants: 116732733-A-G

69825521-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: missense variant
orthologous variants: 116732563-G-C

http://identifiers.org/hco/12/GRCh38#69825593-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#116732494-C-A

69825717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116732367-T-C

69826150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116731560-G-A

69826886-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116730753-T-A

69827312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116730054-G-A

69829361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116729493-G-A

69829365-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116729489-G-C

69829618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116729226-A-G

69829849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116728968-G-A

69829867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116728949-C-T

69830167-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116728693-G-C

69830544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116728585-T-C

69830735-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116728390-G-C

69830800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116728329-C-T

69830893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116728256-A-G

69830957-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116728196-G-C

69831029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116728132-A-G

69831077-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116728088-C-G

69831116-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116728030-T-C

69831357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116727682-A-G

69831541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116727494-A-G

http://identifiers.org/hco/12/GRCh38#69831633-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#116727402-C-A

http://identifiers.org/hco/12/GRCh38#69833571-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#116721395-A-C

http://identifiers.org/hco/12/GRCh38#69833615-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#116721348-A-C

69833711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116721270-C-T

69833802-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116721224-T-A

http://identifiers.org/hco/12/GRCh38#69834060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#116721034-C-A

69834668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116720784-C-T

69834733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116720719-A-G

69835691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116719789-A-G

69836489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116719734-C-T

69836543-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116719682-C-G

69836543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116719682-C-T

69838624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116714077-G-A

69838676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116714026-G-A

69838679-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116714023-T-G

69838714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116713992-C-T

69838770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116713939-G-A

69838887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116713827-A-G

69838996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116713721-A-G

69839026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116713691-G-A

69839148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116713581-G-A

69839293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116713462-C-T

69839908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116711886-C-T

http://identifiers.org/hco/12/GRCh38#69840091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#116711732-C-A

69840091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116711732-C-T

69840155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116711685-C-T

69840227-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116711624-T-A

69840328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116711529-C-T

69840330-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116711527-G-C

69840473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116711151-C-T

69840590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116711030-A-G

69840695-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116710918-C-G

69840704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116710910-G-A

69841298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116710020-G-A

69841570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116709760-A-G

69843815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116708140-G-A

69843922-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116708024-G-C

69843985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116707980-G-A

69844200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116707764-G-A

69844290-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116707682-G-C

69844294-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116707678-G-T

69844394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116707564-C-T

69844480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116707408-C-T

http://identifiers.org/hco/12/GRCh38#69844598-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#116707257-C-A

69844598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116707257-C-T

69844746-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116706900-G-C

69844895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116706746-C-T

69845057-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116706567-T-G

http://identifiers.org/hco/12/GRCh38#69845062-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#116706562-C-A

69845273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116702413-C-T

69845382-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116702296-C-G

69845415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116702263-A-G

http://identifiers.org/hco/12/GRCh38#69845596-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#116702095-A-C

69845662-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116702033-T-G

http://identifiers.org/hco/12/GRCh38#69845812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#116701888-C-A

69845812-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116701888-C-G

69845938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116701741-T-C

69845946-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116701733-C-G

69849679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116699212-G-A

69849679-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116699212-G-C

69855486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116697211-C-T

69855495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116697202-G-A

69865717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116692152-C-T

69865720-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116692149-G-T

69866151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116691755-T-C

69866481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116691459-G-A

69867901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116690499-G-A

69868013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116690397-T-C

69868135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116690381-C-T

69868680-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116690073-T-G

69868694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116690059-C-T

69869368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116689593-C-T

http://identifiers.org/hco/12/GRCh38#69869462-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#116689497-A-C

69869502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116689446-G-A

69869609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116689347-T-C

69869959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116689009-C-T

69870478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116688352-G-A

69878357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116685734-C-T

http://identifiers.org/hco/12/GRCh38#69878945-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#116685423-C-A

69878967-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116685401-G-T

http://identifiers.org/hco/12/GRCh38#69879038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#116685327-C-A

69879038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: missense variant
orthologous variants: 116685327-C-T

69879128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116685238-C-T

69879151-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116685219-T-G

http://identifiers.org/hco/12/GRCh38#69879211-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#116685155-C-A

http://identifiers.org/hco/12/GRCh38#69879220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#116685146-C-A

69879220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: synonymous variant
orthologous variants: 116685146-C-T

69879274-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: missense variant
orthologous variants: 116685092-G-T

69879275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: missense variant
orthologous variants: 116685091-C-T

69879302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: missense variant
orthologous variants: 116685064-T-C

http://identifiers.org/hco/12/GRCh38#69879349-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: stop gained
orthologous variants: http://identifiers.org/mco/10/GRCm39#116685032-C-A

69879353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: missense variant
orthologous variants: 116685028-T-C

69879364-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: missense_variant, undefined
orthologous variants: 116685017-T-A

69879389-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: missense variant
orthologous variants: 116684992-T-G

69879392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: missense variant
orthologous variants: 116684989-G-A

69879507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116684889-G-T

69879574-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116684830-G-T

http://identifiers.org/hco/12/GRCh38#69879583-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#116684821-A-C

69879583-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116684821-A-T

69879593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116684812-G-A

69879646-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116684765-C-G

69880116-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116684354-G-T

69880200-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: splice acceptor variant
orthologous variants: 116684271-G-C

69880266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: missense variant
orthologous variants: 116684205-G-A

69880266-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: missense variant
orthologous variants: 116684205-G-C

69880513-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116683957-G-C

69880545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116683930-G-A

69880560-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116683914-A-T

69880612-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116683869-C-G

69880612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116683869-C-T

69881278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116683655-G-A

69881283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116683650-A-G

69881301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116683632-T-C

69881494-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116683483-C-G

69881505-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116683472-G-T

http://identifiers.org/hco/12/GRCh38#69881506-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#116683471-C-A

69881577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116683404-C-T

69881578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116683403-G-A

69881689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116683266-A-G

69881717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116683238-G-A

69881911-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116683076-G-C

69881911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116683076-G-T

69882298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116682689-A-G

http://identifiers.org/hco/12/GRCh38#69882306-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#116682681-A-C

69882350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116682654-T-C

69882404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116682610-G-A

69882476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116682550-G-A

69882814-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116681355-G-C

http://identifiers.org/hco/12/GRCh38#69882930-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#116681249-C-A

69883132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116681068-A-G

69883182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116681020-C-T

69883184-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116681018-G-C

69883246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116680957-G-A

69883342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116680864-T-C

69884309-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116680116-A-T

http://identifiers.org/hco/12/GRCh38#69884318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#116680107-C-A

69885273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116678874-T-C

69885500-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116678675-C-G

69885500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116678675-C-T

69885545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116678629-C-T

69886052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116676060-G-A

69886080-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116676030-T-A

69886099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116676027-T-C

69886192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116675956-G-A

69886347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116675815-C-T

69886398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116675749-A-G

69886407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116675740-G-A

69886418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116675729-G-A

http://identifiers.org/hco/12/GRCh38#69886782-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#116675428-C-A

69886782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116675428-C-T

http://identifiers.org/hco/12/GRCh38#69886855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#116675353-C-A

69886855-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: missense variant
orthologous variants: 116675353-C-G

69886855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: missense variant
orthologous variants: 116675353-C-T

http://identifiers.org/hco/12/GRCh38#69886989-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#116675216-C-A

http://identifiers.org/hco/12/GRCh38#69887059-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#116675130-C-A

69887059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116675130-C-T

69887132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116675056-A-G

69887810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116674413-T-C

69887857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116674376-T-C

69887904-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116674328-G-T

69887966-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116674269-T-G

http://identifiers.org/hco/12/GRCh38#69888443-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#116673401-A-C

69888521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116673318-A-G

http://identifiers.org/hco/12/GRCh38#69889201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#116671636-C-A

69889842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116671296-C-T

69889980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116671195-T-C

http://identifiers.org/hco/12/GRCh38#69889991-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#116671184-A-C

69889991-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116671184-A-T

69890068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116671108-A-G

69890093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116671084-G-A

http://identifiers.org/hco/12/GRCh38#69890212-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#116670915-C-A

69890314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116670837-G-A

69890380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116670771-T-C

69890826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116670658-A-G

http://identifiers.org/hco/12/GRCh38#69890961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#116670557-C-A

69890961-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116670557-C-G

69891064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: missense variant
orthologous variants: 116670454-G-T

69891104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: missense variant
orthologous variants: 116670414-G-A

69891197-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116670322-A-T

http://identifiers.org/hco/12/GRCh38#69891200-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#116670319-C-A

69893610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116669052-G-A

69893640-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116669017-C-G

http://identifiers.org/hco/12/GRCh38#69893744-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#116668900-C-A

69893744-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116668900-C-G

69893744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116668900-C-T

69893764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 116668871-G-A

69893788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: missense variant
orthologous variants: 116668847-G-A

69893788-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: missense variant
orthologous variants: 116668847-G-C

69893788-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: missense variant
orthologous variants: 116668847-G-T

69893809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: missense variant
orthologous variants: 116668826-G-A

69893809-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: missense variant
orthologous variants: 116668826-G-C

69893809-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: missense variant
orthologous variants: 116668826-G-T

69893844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116668791-A-G

69893866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116668769-T-C

69893882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116668754-A-G

http://identifiers.org/hco/12/GRCh38#69893894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#116668743-C-A

69893894-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116668743-C-G

69893896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116668741-T-C

69893989-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116668678-A-T

69894293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116668495-C-T

69894342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116668446-A-G

69894782-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116668040-C-G

http://identifiers.org/hco/12/GRCh38#69894856-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#116667961-C-A

69894861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116667956-C-T

69894921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116667896-C-T

69894926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116667891-G-A

http://identifiers.org/hco/12/GRCh38#69894953-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#116667864-A-C

69894966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116667850-A-G

69895078-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116667726-C-G

http://identifiers.org/hco/12/GRCh38#69895079-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#116667725-C-A

69895143-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116667665-G-C

69895194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116667630-T-C

69895280-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116667547-T-A

69895280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116667547-T-C

69895280-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116667547-T-G

69895284-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116667545-T-G

69895305-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116667526-G-C

69895305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116667526-G-T

69895315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116667516-G-A

69895315-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116667516-G-T

69895332-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116667501-T-A

69895332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116667501-T-C

69895332-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116667501-T-G

69895333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116667500-A-G

69895376-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: missense variant
orthologous variants: 116667466-A-T

69895517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116667329-G-A

69895517-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116667329-G-T

69895551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116667301-G-A

69895558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116667294-T-C

69895569-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116667283-G-T

http://identifiers.org/hco/12/GRCh38#69895585-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#116667268-C-A

69895585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116667268-C-T

69895603-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116667249-C-G

69895608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116667244-C-T

http://identifiers.org/hco/12/GRCh38#69895617-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#116667235-C-A

69895617-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116667235-C-G

69895692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116667171-C-T

69896285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116666413-G-A

69896285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116666413-G-T

69896804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116665240-A-G

69897033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116665074-T-C

69897033-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116665074-T-G

http://identifiers.org/hco/12/GRCh38#69897034-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#116665073-C-A

69897050-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116665057-T-G

69897084-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116665023-G-T

69897122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116664984-A-G

69897122-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116664984-A-T

69897154-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: splice acceptor variant
orthologous variants: 116664952-A-T

69897272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116664835-G-A

69897272-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116664835-G-T

69897318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116664789-A-G

69897321-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116664780-G-C

69897321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116664780-G-T

69897528-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116664644-C-G

69897579-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116664590-G-C

69897649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116664521-G-A

69897699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116664466-A-G

69897739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116664431-A-G

69897739-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116664431-A-T

69897822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116664337-G-A

69898092-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116664091-A-G

69898317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116663869-G-A

69898396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116663809-C-T

69898685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116663540-A-G

69898919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116663321-A-G

69898965-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116663273-C-G

http://identifiers.org/hco/12/GRCh38#69899266-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#116662978-C-A

69899404-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116662501-G-C

69899659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116662210-T-C

69899709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116662164-C-T

69900467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116661679-G-A

69900772-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116661396-C-G

69900969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116661214-C-T

69901449-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116660552-G-C

69901453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116660548-A-G

69901831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron variant
orthologous variants: 116660189-C-T

69902208-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116660177-T-G

69902393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116659979-A-G

69902443-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116659928-C-G

69903256-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116659147-T-A

69903556-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116658872-T-C

69903577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116658851-A-G

69903726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: missense_variant, undefined
orthologous variants: 116658704-G-A

69903752-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: missense_variant, undefined
orthologous variants: 116658678-C-G

http://identifiers.org/hco/12/GRCh38#69903935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#116658044-C-A

69903935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116658044-C-T

http://identifiers.org/hco/12/GRCh38#69903995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#116657980-C-A

69903995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116657980-C-T

http://identifiers.org/hco/12/GRCh38#69904006-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#116657969-C-A

http://identifiers.org/hco/12/GRCh38#69905448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#116657334-C-A

69905449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116657333-C-T

69905463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116657319-G-A

69905469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116657313-A-G

69905757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116657035-T-C

69909933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116653731-A-G

http://identifiers.org/hco/12/GRCh38#69909978-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#116653686-A-C

69909978-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 116653686-A-T

69910089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116653575-A-G

69910103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116653561-T-C

http://identifiers.org/hco/12/GRCh38#69910113-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#116653551-C-A

69910132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116653532-T-C

69910202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116653473-G-T

69910213-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116653462-T-G

69910255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116653409-A-G

69910284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116653381-G-T

69910388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116653318-G-A

69910408-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116653296-T-A

69910415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116653289-A-G

http://identifiers.org/hco/12/GRCh38#69910602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#116653072-C-A

69910610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116653046-T-C

69910651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116653006-A-G

69910658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116652999-G-A

69910658-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116652999-G-T

69910691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116652962-A-G

http://identifiers.org/hco/12/GRCh38#69910799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#116652826-C-A

69910799-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116652826-C-G

69910799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116652826-C-T

69910966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116652655-T-C

69910977-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116652645-A-T

69911150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116652467-A-G

69911276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116652332-A-G

69911582-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116651813-C-G

69911582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116651813-C-T

69911665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116651727-C-T

69911744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116651649-A-G

69911755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116651642-T-C

69917341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116649778-G-A

http://identifiers.org/hco/12/GRCh38#69917409-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#116649729-C-A

69917409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116649729-C-T

69917419-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116649719-T-A

69917419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116649719-T-C

69917524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116649611-G-A

69917577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116649558-T-C

69917590-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116649545-T-A

69917930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116649277-A-G

69917966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116649250-G-A

http://identifiers.org/hco/12/GRCh38#69917978-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#116649238-C-A

69917978-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116649238-C-G

69918014-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116649205-G-C

69918014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116649205-G-T

69918103-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116649114-T-A

69918148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116649068-G-A

69918905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116647086-G-A

69921130-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116646469-G-C

69921497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116646053-T-C

69921872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116645715-C-T

http://identifiers.org/hco/12/GRCh38#69922213-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#116645409-A-C

69922254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116645371-T-C

69922323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116645301-A-G

69922376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116645260-C-T

69922445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116645197-A-G

http://identifiers.org/hco/12/GRCh38#69925966-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#116640117-A-C

69926014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116640066-G-A

http://identifiers.org/hco/12/GRCh38#69926031-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#116640049-A-C

http://identifiers.org/hco/12/GRCh38#69926074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#116640004-C-A

69926139-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116639932-T-A

69926139-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116639932-T-G

69926140-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116639931-T-A

69926140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116639931-T-C

69926140-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116639931-T-G

69926150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116639921-G-A

69926150-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116639921-G-C

69926150-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116639921-G-T

69926159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116639913-T-C

69926159-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116639913-T-G

69926303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116639720-A-G

http://identifiers.org/hco/12/GRCh38#69926384-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#116639632-C-A

http://identifiers.org/hco/12/GRCh38#69926424-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#116639592-C-A

69926424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116639592-C-T

69926471-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116639565-T-G

69926477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116639559-A-G

http://identifiers.org/hco/12/GRCh38#69926489-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#116639551-C-A

69926501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116639539-G-A

69926501-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116639539-G-T

69926503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116639537-G-A

69926503-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116639537-G-T

http://identifiers.org/hco/12/GRCh38#69926526-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#116639514-C-A

69926526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116639514-C-T

69926736-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, splice_donor_variant, undefined
orthologous variants: 116639300-T-A

69926736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, splice_donor_variant, undefined
orthologous variants: 116639300-T-C

69926737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116639299-A-G

69926737-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116639299-A-T

http://identifiers.org/hco/12/GRCh38#69926738-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#116639298-C-A

69926738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116639298-C-T

69926922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116639132-T-C

69927297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116639081-G-A

69927404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116638961-A-G

69927443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116638922-A-G

69927469-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116638896-G-T

69927605-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116638744-G-T

69927617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116638734-C-T

69927715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 116638632-T-C

69927782-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116638564-T-A

69930052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116636268-G-A

69930065-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116636255-C-G

69930337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116636045-G-A

69930374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116636008-C-T

69931349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116635935-G-A

69931351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116635933-A-G

69931402-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116635882-A-T

69931441-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116635844-G-C

69931486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116635808-T-C

69931803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116635138-C-T

69932452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116634621-G-A

69932452-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116634621-G-C

http://identifiers.org/hco/12/GRCh38#69932646-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#116634445-C-A

69932646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116634445-C-T

http://identifiers.org/hco/12/GRCh38#69932647-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#116634444-C-A

69932669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116634434-G-T

69932727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116634385-A-G

69932748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116634364-G-A

69932748-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116634364-G-C

69932748-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116634364-G-T

69932810-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116634314-G-C

69932863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116634280-G-A

69932885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116634258-G-T

69932887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116634256-G-A

69932889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116634254-G-A

69932889-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116634254-G-T

69933166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116633983-A-G

69933755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116633299-C-T

69934103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116632973-A-G

69935675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116632445-T-C

69935688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116632433-G-A

69935904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116632245-C-T

http://identifiers.org/hco/12/GRCh38#69935947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#116632189-C-A

69935947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116632189-C-T

69936042-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116632096-T-A

69936064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116632070-A-G

http://identifiers.org/hco/12/GRCh38#69936066-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#116632068-C-A

http://identifiers.org/hco/12/GRCh38#69936073-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#116632061-A-C

69936073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116632061-A-G

69936073-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116632061-A-T

69936126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 116632024-G-A

69936126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 116632024-G-T

69936314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 116631646-C-T

69936357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116631604-C-T

69936460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 116631518-T-C

69936512-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 116631466-T-C

http://identifiers.org/hco/12/GRCh38#69936524-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#116631454-C-A

69936539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 116631439-T-C

69936555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 116631423-G-A

69936599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 116631379-G-A

69936612-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 116631363-T-A

http://identifiers.org/hco/12/GRCh38#69936715-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#116631261-A-C

69936715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116631261-A-G

69936715-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116631261-A-T

69936778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116631204-A-G

69936876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116631121-T-C

69936895-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116631105-A-T

http://identifiers.org/hco/12/GRCh38#69936952-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#116631004-C-A

69936952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116631004-C-T

69937078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116630775-A-G

69937519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116630047-A-G

69937519-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116630047-A-T

69937900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116629154-G-A

69937972-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116629085-T-A

69938049-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116629002-G-C

69938112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116628906-C-T

http://identifiers.org/hco/12/GRCh38#69946090-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#116630293-A-C

69946469-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116627889-T-A

69946476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116627882-C-T

69946614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116627752-C-T

69946644-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116627722-G-T

http://identifiers.org/hco/12/GRCh38#69946839-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#116627592-C-A

http://identifiers.org/hco/12/GRCh38#69946851-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#116627580-C-A

69946861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116627570-A-G

69946904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116627528-A-G

69946925-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116627507-G-T

69946957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116627465-C-T

http://identifiers.org/hco/12/GRCh38#69946973-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#116627431-C-A

69946989-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116627414-G-T

69947007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116627396-T-C

http://identifiers.org/hco/12/GRCh38#69947031-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#116627372-C-A

http://identifiers.org/hco/12/GRCh38#69947265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#116626914-C-A

69947360-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116626819-G-C

69947750-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116626463-C-G

69947819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116626400-A-G

69947918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116626310-G-A

69948068-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116626167-T-A

69948068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116626167-T-C

69948087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116626147-G-A

69948218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116626050-G-A

69948218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116626050-G-T

69949006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116623417-A-G

69949096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116623333-G-A

69949241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116623178-A-G

69950376-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116620475-A-T

69950459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116620375-C-T

69950696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116620185-T-C

69950788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116620099-G-A

69950788-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116620099-G-T

69950790-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116620097-G-C

69951067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116619872-A-G

69951207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116619751-C-T

69951306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116619647-G-T

69951357-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116619598-G-C

69951775-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116619487-C-G

69951954-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116619324-G-C

69951965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116619313-A-G

69951981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116619276-G-A

69951993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116619264-G-A

69951993-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116619264-G-T

69952000-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116619235-G-T

69952029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116619206-A-G

69952227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116619016-A-G

http://identifiers.org/hco/12/GRCh38#69952329-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#116618436-C-A

69952329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116618436-C-T

http://identifiers.org/hco/12/GRCh38#69952354-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#116618411-A-C

69952354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116618411-A-G

69952645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116618104-C-T

http://identifiers.org/hco/12/GRCh38#69952674-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#116618080-A-C

69952736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116618020-A-G

69952759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116617999-A-G

http://identifiers.org/hco/12/GRCh38#69952786-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#116617952-C-A

69952786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116617952-C-T

69952923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116617816-G-A

69952923-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116617816-G-T

69952942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116617799-G-T

http://identifiers.org/hco/12/GRCh38#69952972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#116617769-C-A

http://identifiers.org/hco/12/GRCh38#69953000-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#116617741-A-C

http://identifiers.org/hco/12/GRCh38#69953392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#116617369-C-A

69953455-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116617307-T-G

69954021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116616894-T-C

69954190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116616721-G-A

69954293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116616607-G-A

http://identifiers.org/hco/12/GRCh38#69954353-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#116616549-A-C

69954576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116616251-C-T

69954817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116616011-G-A

69954854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116615973-A-G

69954966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116615862-G-A

69955014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116615822-G-A

69955218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116615668-A-G

69955321-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116615567-T-C

69955321-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116615567-T-G

69955332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116615556-A-G

69955442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116615447-G-A

69955448-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116615441-G-T

69955480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116615410-G-A

69955480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116615410-G-T

69955501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116615389-T-C

69955520-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116615374-T-A

69955520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116615374-T-C

69955696-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116615246-A-T

69955756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116615197-A-G

69955776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116615177-C-T

69955945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116614971-C-T

http://identifiers.org/hco/12/GRCh38#69957743-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#116613428-C-A

69957743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116613428-C-T

http://identifiers.org/hco/12/GRCh38#69957784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#116613387-C-A

69957798-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116613379-C-G

69957798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116613379-C-T

69957813-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116613367-C-G

69957813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116613367-C-T

http://identifiers.org/hco/12/GRCh38#69957833-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#116613347-C-A

69957963-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116613179-T-G

http://identifiers.org/hco/12/GRCh38#69958115-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#116613059-A-C

69958168-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116613006-A-T

http://identifiers.org/hco/12/GRCh38#69958202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#116612971-C-A

69958213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116612960-G-A

http://identifiers.org/hco/12/GRCh38#69958229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#116612946-C-A

69958229-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116612946-C-G

69958229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116612946-C-T

69958273-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 116612902-C-G

69958273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 116612902-C-T

69958288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 116612887-T-C

69958297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 116612878-A-G

69958297-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 116612878-A-T

69958389-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116612764-A-T

69958427-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116612726-T-A

69958427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, undefined
orthologous variants: 116612726-T-C

69958451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 116612711-G-A

69958496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 116612666-G-A

69958496-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 116612666-G-T

http://identifiers.org/hco/12/GRCh38#69958578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#116612581-C-A

69958578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 116612581-C-T

69958689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 116612478-A-G

69958734-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 116612433-A-T

69958749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 116612417-A-G

http://identifiers.org/hco/12/GRCh38#69958844-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#116612339-A-C

http://identifiers.org/hco/12/GRCh38#69958969-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#116612231-A-C

69958969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 116612231-A-G

69958969-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 116612231-A-T

69958982-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 116612214-T-G

http://identifiers.org/hco/12/GRCh38#69959041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#116612137-C-A

http://identifiers.org/hco/12/GRCh38#69959056-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26316
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#116612110-A-C