http://identifiers.org/hco/8/GRCh38#109362472-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44320838-C-A

109362472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: 5 prime UTR variant
orthologous variants: 44320838-C-T

109362531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: 5 prime UTR variant
orthologous variants: 44320895-T-C

http://identifiers.org/hco/8/GRCh38#109362562-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44320930-C-A

109362562-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: 5 prime UTR variant
orthologous variants: 44320930-C-G

109362562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: 5 prime UTR variant
orthologous variants: 44320930-C-T

http://identifiers.org/hco/8/GRCh38#109362563-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44320931-C-A

109362563-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: 5 prime UTR variant
orthologous variants: 44320931-C-G

109362563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: 5 prime UTR variant
orthologous variants: 44320931-C-T

109362567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: 5 prime UTR variant
orthologous variants: 44320935-G-A

109362567-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: 5 prime UTR variant
orthologous variants: 44320935-G-C

109362567-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: 5 prime UTR variant
orthologous variants: 44320935-G-T

109362599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: synonymous variant
orthologous variants: 44320967-C-T

http://identifiers.org/hco/8/GRCh38#109362646-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44321014-C-A

109362646-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: synonymous variant
orthologous variants: 44321014-C-G

109362646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: synonymous variant
orthologous variants: 44321014-C-T

http://identifiers.org/hco/8/GRCh38#109362710-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44321061-C-A

109362710-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44321061-C-G

109362710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44321061-C-T

109362765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44321115-G-A

http://identifiers.org/hco/8/GRCh38#109362781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44321117-C-A

109362781-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44321117-C-G

109362781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44321117-C-T

109362796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44321132-G-T

109362798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44321134-G-A

109362798-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44321134-G-C

109362849-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44321197-C-G

109362903-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44321273-A-T

109363095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, undefined
orthologous variants: 44321444-G-A

109363096-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, undefined
orthologous variants: 44321445-T-G

109363170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44321514-A-G

109363284-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44321631-T-A

109363381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44321725-G-A

http://identifiers.org/hco/8/GRCh38#109364013-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44322337-A-C

109364013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44322337-A-G

109364075-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44322394-T-A

109364075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44322394-T-C

109364083-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44322402-T-A

109364209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44322510-T-C

109364261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44322561-C-T

http://identifiers.org/hco/8/GRCh38#109364464-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44322719-C-A

109364464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44322719-C-T

109364671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44322955-G-A

109364671-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44322955-G-T

http://identifiers.org/hco/8/GRCh38#109364689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44322979-C-A

109364689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44322979-C-T

109364895-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44323299-C-G

http://identifiers.org/hco/8/GRCh38#109364896-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44323300-A-C

109364904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44323313-C-T

109364914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44323323-A-G

109364948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44323360-T-C

109365037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44323437-G-A

109365123-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44323527-C-G

109365241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44323633-A-G

109365304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44323714-C-T

109365307-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44323717-T-A

109365551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44323948-A-G

109365985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44324105-G-A

109365985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44324105-G-T

109365988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44324108-A-G

109366021-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44324141-C-G

109366044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44324161-T-C

109366670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44324790-A-G

http://identifiers.org/hco/8/GRCh38#109367461-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44325045-C-A

http://identifiers.org/hco/8/GRCh38#109367569-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44325133-A-C

109367954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44325302-G-A

109367959-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44325307-T-G

109368050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44325381-G-A

109368129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44325459-T-C

109368209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44325515-T-C

109368452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44325734-T-C

109368452-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44325734-T-G

109368462-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44325744-G-C

109368551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44325946-G-A

http://identifiers.org/hco/8/GRCh38#109368606-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44326138-C-A

109368787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44326308-G-A

109368787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44326308-G-T

109368867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44326389-C-T

109369238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44326680-A-G

http://identifiers.org/hco/8/GRCh38#109369269-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44326715-A-C

109369403-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44326829-A-T

109369472-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44326893-T-A

109369534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44326950-G-A

http://identifiers.org/hco/8/GRCh38#109369668-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44327071-C-A

109369876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44327296-T-C

109369939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44327358-G-A

109376991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44327709-A-G

109377372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44327983-A-G

109377591-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44328153-T-A

109377616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44328178-T-C

109377706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44328258-G-A

109380003-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44328715-C-G

109380003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44328715-C-T

109380041-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44328753-G-T

109381194-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44329505-G-T

109381238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44329546-A-G

109381251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44329559-T-C

http://identifiers.org/hco/8/GRCh38#109381260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44329570-C-A

109381267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44329577-G-T

http://identifiers.org/hco/8/GRCh38#109381284-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44329592-C-A

109381284-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44329592-C-G

109381284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44329592-C-T

109381362-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 44329666-T-A

109381362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 44329666-T-C

109381401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: synonymous variant
orthologous variants: 44329705-A-G

109381401-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: synonymous variant
orthologous variants: 44329705-A-T

109381403-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense variant
orthologous variants: 44329707-T-A

109381403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense variant
orthologous variants: 44329707-T-C

http://identifiers.org/hco/8/GRCh38#109381566-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44329868-C-A

109381566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44329868-C-T

109381600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44329902-A-G

109381637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44329937-G-A

109381637-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44329937-G-C

109381637-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44329937-G-T

109381643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44329943-A-G

109381661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44329961-T-C

109381794-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44330099-T-A

109381871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44330176-G-A

109381944-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44330248-T-A

109382063-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44330354-G-C

109382122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44330411-A-G

http://identifiers.org/hco/8/GRCh38#109382148-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44330437-C-A

109382148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44330437-C-T

109382278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44330558-A-G

109382279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44330559-T-C

109382324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44330602-A-G

109382340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44330618-G-A

109382340-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44330618-G-T

109382352-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44330628-G-T

109382559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: synonymous variant
orthologous variants: 44330831-A-G

109382603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44330874-T-C

109382603-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44330874-T-G

109382625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44330890-T-C

109382625-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44330890-T-G

109382637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44330902-T-C

109382651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44330916-T-C

109382679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44330950-T-C

109382686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44330957-G-A

109382686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44330957-G-T

109382721-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44330978-T-G

http://identifiers.org/hco/8/GRCh38#109382817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44331063-C-A

109383982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44340846-A-G

109384003-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44340860-T-C

109384004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44340861-A-G

109384010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44340867-T-C

109384010-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44340867-T-G

109384040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44340914-G-A

http://identifiers.org/hco/8/GRCh38#109384072-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44340950-A-C

109384072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 44340950-A-G

http://identifiers.org/hco/8/GRCh38#109384087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44340965-C-A

http://identifiers.org/hco/8/GRCh38#109384141-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44341019-C-A

109384141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44341019-C-T

109385413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44342872-G-T

http://identifiers.org/hco/8/GRCh38#109385664-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44343132-C-A

http://identifiers.org/hco/8/GRCh38#109385666-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44343134-C-A

109385668-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44343136-T-A

109385668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44343136-T-C

109385767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44343219-T-C

109385914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44343300-G-A

109386227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44344729-G-A

109386343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44344843-C-T

109386371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44344871-G-A

109386489-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44345003-C-G

109386489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44345003-C-T

109386566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44345077-A-G

109386714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44345206-C-T

109386716-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44345208-T-G

109386719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44345211-A-G

109386756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44345248-C-T

109386840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44345553-T-C

109386985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44345696-T-C

109387133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44345816-T-C

109387610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44346352-A-G

109387720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44346631-T-C

109387722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44346633-T-C

109387734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44346645-T-C

109387833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44346732-G-T

109388104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44346860-C-T

109388376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44347094-G-A

109388376-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44347094-G-T

109388506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: synonymous variant
orthologous variants: 44347214-T-C

109388506-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense variant
orthologous variants: 44347214-T-G

109388621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44347316-T-C

http://identifiers.org/hco/8/GRCh38#109388693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44347376-C-A

109388693-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44347376-C-G

109388857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44347537-A-G

109388903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44347580-T-C

http://identifiers.org/hco/8/GRCh38#109388966-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44347642-C-A

109389018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44347693-A-G

http://identifiers.org/hco/8/GRCh38#109389043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44347712-C-A

109389070-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44347741-T-G

109389166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44347837-A-G

109389224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44347880-A-G

http://identifiers.org/hco/8/GRCh38#109389235-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44347894-C-A

109389235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44347894-C-T

http://identifiers.org/hco/8/GRCh38#109389242-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44347901-C-A

109389242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44347901-C-T

109389244-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44347903-T-A

109389388-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44347994-C-G

109389388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44347994-C-T

http://identifiers.org/hco/8/GRCh38#109389407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44348021-C-A

109389407-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44348021-C-G

109389407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44348021-C-T

109389684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44348176-T-C

109389684-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44348176-T-G

109389758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44348197-C-T

109389776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44348215-C-T

http://identifiers.org/hco/8/GRCh38#109389969-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44348361-A-C

109389999-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44348387-T-G

109390027-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44348413-G-T

109390030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44348416-A-G

109390075-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44348459-C-G

109390275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44348646-A-G

109390344-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44348707-T-G

109390358-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44348715-T-A

109390358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44348715-T-C

109390371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44348728-T-C

109390376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44348733-T-C

109390388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44348744-T-C

http://identifiers.org/hco/8/GRCh38#109390391-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44348747-A-C

109390391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44348747-A-G

109390528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44348879-T-C

http://identifiers.org/hco/8/GRCh38#109390702-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44349070-A-C

109390768-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44349153-C-G

109390834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44349417-A-G

109390834-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44349417-A-T

109390869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44349448-A-G

109391063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44349620-A-G

109391094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44349649-T-C

109391284-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44349796-C-G

109391574-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44350063-T-A

109391574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44350063-T-C

109391624-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44350117-T-A

109391648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44350141-T-C

109391693-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44350183-C-G

109392147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44350668-C-T

109392552-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44351206-G-T

109392608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44351277-T-C

109392673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44351352-T-C

http://identifiers.org/hco/8/GRCh38#109392711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44351412-C-A

109392725-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44351425-T-A

109392725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44351425-T-C

109392867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44351589-C-T

109392926-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44351648-G-C

109393170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44351890-T-C

109393330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44352052-T-C

109393388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44352114-T-C

109393461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44352190-A-G

109393590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44352336-G-A

109393809-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44352558-G-T

109393816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44352565-G-A

109393853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44352603-A-G

109394219-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44352682-T-A

109394219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44352682-T-C

109394228-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44352691-A-G

109394278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44352748-A-G

109394279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44352749-A-G

109394280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44352750-G-A

109394280-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44352750-G-T

http://identifiers.org/hco/8/GRCh38#109394323-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44352799-C-A

109394388-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44352878-G-T

109394404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44352895-T-C

109394448-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: synonymous variant
orthologous variants: 44352944-T-A

109394448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: synonymous variant
orthologous variants: 44352944-T-C

109394448-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: synonymous variant
orthologous variants: 44352944-T-G

109394537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44353025-T-C

109394549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44353037-T-C

109394585-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44353075-T-A

109394633-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44353116-A-G

109394649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44353132-A-G

109394713-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44353179-C-G

109394723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44353189-A-G

109394763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44353229-A-G

109394768-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44353234-T-A

109394768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44353234-T-C

109395175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44353570-G-A

109396042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense variant
orthologous variants: 44354437-T-C

http://identifiers.org/hco/8/GRCh38#109396070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44354465-C-A

109396070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: synonymous variant
orthologous variants: 44354465-C-T

109396073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: synonymous variant
orthologous variants: 44354468-C-T

109396143-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44354538-T-A

109396150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44354545-G-A

http://identifiers.org/hco/8/GRCh38#109396186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44354581-C-A

109396186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44354581-C-T

109396199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44354594-A-G

109396215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44354607-A-G

http://identifiers.org/hco/8/GRCh38#109396299-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44354686-A-C

109396590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44354927-C-T

109396614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44354951-G-A

109396637-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44354968-G-C

109396637-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44354968-G-T

109396656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44354987-G-A

109396656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44354987-G-T

109396870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44355204-C-T

109398073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44355545-A-G

109398134-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44355601-G-C

109398234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44355710-C-T

http://identifiers.org/hco/8/GRCh38#109398262-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44355738-A-C

http://identifiers.org/hco/8/GRCh38#109398378-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44356378-C-A

109398407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44356408-T-C

109398428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44356428-A-G

109398429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44356429-G-A

109398529-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: synonymous variant
orthologous variants: 44356529-T-A

http://identifiers.org/hco/8/GRCh38#109398530-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44356530-C-A

109398530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense variant
orthologous variants: 44356530-C-T

109398540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense variant
orthologous variants: 44356540-T-C

http://identifiers.org/hco/8/GRCh38#109398558-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44356558-C-A

109398558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44356558-C-T

109398563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44356563-G-A

109398563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44356563-G-T

109398572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44356572-G-A

109398572-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44356572-G-T

109398591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44356591-A-G

109398591-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44356591-A-T

http://identifiers.org/hco/8/GRCh38#109398612-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44356611-A-C

109398612-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44356611-A-T

109398619-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44356618-T-A

109398619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44356618-T-C

109399038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44357673-A-G

109399063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44357702-T-C

109399063-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44357702-T-G

109399110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44357739-G-A

109399152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44357777-G-A

109399236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44357861-T-C

109399330-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44357964-T-A

109399402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44358032-G-A

109399449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44358090-T-C

109399536-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44358247-G-C

109399716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44358438-C-T

109399814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44358549-A-G

109400039-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44358768-T-G

http://identifiers.org/hco/8/GRCh38#109400041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44358770-C-A

109400197-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: synonymous variant
orthologous variants: 44358926-C-G

109400197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: synonymous variant
orthologous variants: 44358926-C-T

109401337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44359397-A-G

109401429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44359483-T-C

109401491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 44359532-G-A

109401491-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 44359532-G-T

109401514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: synonymous variant
orthologous variants: 44359555-T-C

109401605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44359652-T-C

109401693-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44359732-T-A

109401716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44359755-G-A

http://identifiers.org/hco/8/GRCh38#109401722-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44359761-C-A

109401723-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44359863-T-A

109401723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44359863-T-C

http://identifiers.org/hco/8/GRCh38#109404550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44361321-C-A

109404550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 44361321-C-T

109404766-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44361539-T-A

109404790-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44361564-T-A

109404790-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44361564-T-G

109404803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44361593-G-T

http://identifiers.org/hco/8/GRCh38#109404821-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44361625-C-A

http://identifiers.org/hco/8/GRCh38#109404827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44361629-C-A

109404827-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44361629-C-G

109404829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44361631-A-G

109404856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44361695-G-A

109404856-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44361695-G-T

109404868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44361735-A-G

109404896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44361763-A-G

109404956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44361822-T-C

109405011-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense variant
orthologous variants: 44361878-A-T

109405040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense variant
orthologous variants: 44361907-G-A

109405040-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense variant
orthologous variants: 44361907-G-T

109405119-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense variant
orthologous variants: 44361986-T-A

109405119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense variant
orthologous variants: 44361986-T-C

http://identifiers.org/hco/8/GRCh38#109405163-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44362029-C-A

109405163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44362029-C-T

109405165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44362031-G-A

109405170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44362036-T-C

109405170-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44362036-T-G

109405190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44362056-G-A

109405229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44362093-G-A

109405229-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44362093-G-C

http://identifiers.org/hco/8/GRCh38#109405256-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44362120-C-A

109405256-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44362120-C-G

109405256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44362120-C-T

109405271-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44362133-T-A

109405271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44362133-T-C

109405328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44362181-C-T

109406025-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44362410-C-G

109406025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44362410-C-T

109406083-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44362454-G-T

109406203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44362532-A-G

http://identifiers.org/hco/8/GRCh38#109406209-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44362538-A-C

109406227-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44362556-T-A

109406227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44362556-T-C

http://identifiers.org/hco/8/GRCh38#109406272-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44362590-C-A

http://identifiers.org/hco/8/GRCh38#109406340-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44362650-C-A

109406340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: synonymous variant
orthologous variants: 44362650-C-T

109407381-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44362825-A-T

http://identifiers.org/hco/8/GRCh38#109407423-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44362863-C-A

109407423-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44362863-C-G

109407576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44362968-C-T

109407583-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44362975-G-T

109407630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44363021-C-T

109407760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44363139-T-C

109407908-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44363282-T-A

109407908-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44363282-T-G

http://identifiers.org/hco/8/GRCh38#109407962-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44363336-C-A

109408164-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: synonymous variant
orthologous variants: 44363510-G-T

109408260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44363605-T-C

http://identifiers.org/hco/8/GRCh38#109408268-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44363613-C-A

109408268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44363613-C-T

109408304-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44363646-A-T

109408396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44363735-C-T

http://identifiers.org/hco/8/GRCh38#109408480-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44363817-C-A

http://identifiers.org/hco/8/GRCh38#109408489-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44363824-C-A

109408494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44363829-T-C

109408502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44363837-T-C

109408604-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44363930-T-A

109408604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44363930-T-C

109408802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44363959-T-C

109408852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44364008-C-T

109408877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44364022-G-A

109408977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44364127-T-C

109409065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44364222-T-C

109409308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44364400-G-A

109409488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44364438-T-C

109409489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44364439-C-T

109409630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44364587-T-C

109409808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44364778-A-G

109409811-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44364781-A-T

109409906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 44364875-A-G

109409960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 44364929-T-C

109411587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44365999-A-G

109411946-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44366303-C-G

109411946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44366303-C-T

http://identifiers.org/hco/8/GRCh38#109412043-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44366396-A-C

http://identifiers.org/hco/8/GRCh38#109412136-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44366484-C-A

109412294-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: synonymous variant
orthologous variants: 44366638-T-A

109413124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44367060-C-T

109413153-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44367089-T-C

109413289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44367204-T-C

http://identifiers.org/hco/8/GRCh38#109413293-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44367208-C-A

109413293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44367208-C-T

109413299-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44367214-T-A

109413299-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44367214-T-G

http://identifiers.org/hco/8/GRCh38#109413300-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44367215-C-A

109413300-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44367215-C-G

109413300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44367215-C-T

109413317-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44367232-G-C

109413317-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44367232-G-T

109413323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44367237-G-A

109413323-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44367237-G-T

109413357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44367275-G-A

109413357-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44367275-G-T

109413363-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44367281-T-A

109413363-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44367281-T-G

109413391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44367309-G-A

109413391-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44367309-G-T

109413405-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44367323-T-A

109413405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44367323-T-C

109413418-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 44367336-T-A

109413418-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 44367336-T-C

109413461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense variant
orthologous variants: 44367379-G-T

http://identifiers.org/hco/8/GRCh38#109413533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44367451-C-A

109413533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense variant
orthologous variants: 44367451-C-T

109419154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: synonymous variant
orthologous variants: 44368601-A-G

109419202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: synonymous variant
orthologous variants: 44368649-G-A

109419202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense variant
orthologous variants: 44368649-G-T

109419286-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44368733-T-C

http://identifiers.org/hco/8/GRCh38#109420535-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44368898-C-A

109420535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense variant
orthologous variants: 44368898-C-T

109420809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44369166-A-G

109423935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44373875-T-C

109423937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44373877-G-A

109423969-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44373909-A-T

109423992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44373938-A-G

109424197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44374093-T-C

109424976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44374836-A-G

109425019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44374878-G-A

http://identifiers.org/hco/8/GRCh38#109425092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44374951-C-A

109425092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, missense_variant
orthologous variants: 44374951-C-T

http://identifiers.org/hco/8/GRCh38#109425107-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44374966-A-C

109425107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, missense_variant
orthologous variants: 44374966-A-G

109425171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 44375030-A-G

http://identifiers.org/hco/8/GRCh38#109425266-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44375140-C-A

109425266-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44375140-C-G

109425266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44375140-C-T

http://identifiers.org/hco/8/GRCh38#109425326-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44375188-C-A

109425326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44375188-C-T

109425329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44375191-A-G

109425337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44375200-A-G

109425436-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44375268-T-A

109425493-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44375317-T-G

109425542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44375366-A-G

109425601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44375425-G-A

109425626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44375452-G-A

109425752-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44375583-T-A

109425808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44375642-G-A

109425894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44375710-A-G

109425987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44375765-T-C

109426008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44375790-T-C

109426008-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44375790-T-G

109426090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44375861-G-A

109426124-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44375895-T-A

109426124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44375895-T-C

http://identifiers.org/hco/8/GRCh38#109426205-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44375969-A-C

http://identifiers.org/hco/8/GRCh38#109426953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44376151-C-A

109426953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44376151-C-T

109426954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44376152-G-A

109426954-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44376152-G-C

109426998-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 44376181-G-C

109427002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, missense_variant, splice_region_variant
orthologous variants: 44376185-G-A

109427002-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, missense_variant, splice_region_variant
orthologous variants: 44376185-G-T

109427104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, missense_variant
orthologous variants: 44376287-A-G

109427133-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, missense_variant
orthologous variants: 44376316-T-G

http://identifiers.org/hco/8/GRCh38#109427138-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44376321-A-C

109427161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44376344-C-T

109427211-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44376400-G-T

109427246-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44376435-G-T

109428161-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44377257-T-A

109428237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44377328-T-C

109428316-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44377407-G-T

109428426-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44377490-A-T

109428639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44377666-C-T

109428770-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44377792-C-G

109429212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44378137-G-A

109429212-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44378137-G-T

http://identifiers.org/hco/8/GRCh38#109429252-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44378179-C-A

109429252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44378179-C-T

109429316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44378224-T-C

109429446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense variant
orthologous variants: 44378354-C-T

109429573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44378482-G-A

109429585-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44378492-T-A

http://identifiers.org/hco/8/GRCh38#109429720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44378616-C-A

109429720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44378616-C-T

http://identifiers.org/hco/8/GRCh38#109430057-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44379841-C-A

109430057-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44379841-C-G

109430057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44379841-C-T

109430087-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44379950-A-T

109430121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44379978-T-C

http://identifiers.org/hco/8/GRCh38#109430140-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44379997-C-A

109430140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44379997-C-T

109430155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44380012-A-G

109430265-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44380104-T-A

109430321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44380143-G-A

109430617-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44380374-C-G

http://identifiers.org/hco/8/GRCh38#109430703-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44380456-A-C

109430718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44380471-T-C

109432787-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44381199-A-T

109432806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44381218-G-A

109432940-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44381335-A-T

http://identifiers.org/hco/8/GRCh38#109432972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44381366-C-A

109432972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44381366-C-T

109433159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense variant
orthologous variants: 44381558-A-G

109433267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44381666-G-A

109433291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44381684-A-G

109433292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44381685-T-C

109433294-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44381687-A-T

109433437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44381859-C-T

109433444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44381866-C-T

109433509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44381937-G-A

109433629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44382181-T-C

109433692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44382240-A-G

109433802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44382346-C-T

109435025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44382895-A-G

109435074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44382946-G-A

109435074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44382946-G-T

http://identifiers.org/hco/8/GRCh38#109435152-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44383049-A-C

109435167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44383064-C-T

109435303-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense variant
orthologous variants: 44383196-G-C

109435379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44383271-G-A

109435385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44383277-A-G

109435385-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44383277-A-T

109435464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44383360-G-A

109435464-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44383360-G-C

109435464-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44383360-G-T

http://identifiers.org/hco/8/GRCh38#109436099-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44383943-A-C

109436165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44383965-G-A

109436194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44383988-G-A

109436194-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44383988-G-T

109436206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44384000-A-G

109436231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44384014-A-G

109436430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: synonymous variant
orthologous variants: 44384209-T-C

109436430-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense variant
orthologous variants: 44384209-T-G

109436514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44384294-T-C

109436514-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44384294-T-G

109436586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44384359-T-C

http://identifiers.org/hco/8/GRCh38#109436632-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44384404-A-C

109436805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44384569-A-G

109436819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44384582-A-G

109437211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44384869-G-A

109437745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44385187-C-T

109437834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44385266-G-A

109438015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44385430-A-G

109438061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44385482-A-G

http://identifiers.org/hco/8/GRCh38#109438173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44385588-C-A

109438173-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44385588-C-G

109438209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44385623-G-T

109438533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44386546-T-C

109438541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44386554-G-A

109438579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44386587-A-G

109438625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44386633-A-G

http://identifiers.org/hco/8/GRCh38#109438797-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44386788-A-C

http://identifiers.org/hco/8/GRCh38#109438860-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44386847-A-C

109438860-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44386847-A-T

109439051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: synonymous variant
orthologous variants: 44387040-T-C

109439051-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense variant
orthologous variants: 44387040-T-G

109439057-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: stop gained
orthologous variants: 44387046-T-A

109439057-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: synonymous variant
orthologous variants: 44387046-T-C

109439057-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: stop gained
orthologous variants: 44387046-T-G

109439098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44387087-A-G

109439113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44387106-T-C

109439162-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44387152-G-T

109439185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44387177-G-A

109439228-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44387221-A-G

109439230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44387223-G-A

109439230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44387223-G-T

109439353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44387339-C-T

109439362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44387348-C-T

109439363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44387349-A-G

109439363-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44387349-A-T

109439393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44387385-G-T

109439606-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44387565-G-T

109439682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44387630-G-A

109439861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44387795-G-A

109440242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44388182-A-G

109440461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44388391-T-C

http://identifiers.org/hco/8/GRCh38#109440828-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44388716-C-A

109440828-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense variant
orthologous variants: 44388716-C-G

109440885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44388777-A-G

109440903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44388795-G-A

109440903-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44388795-G-T

109440970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44389032-A-G

109441174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44389267-G-A

109441174-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44389267-G-T

http://identifiers.org/hco/8/GRCh38#109441288-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: stop gained
orthologous variants: http://identifiers.org/mco/15/GRCm39#44389356-C-A

109441288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: synonymous variant
orthologous variants: 44389356-C-T

http://identifiers.org/hco/8/GRCh38#109441490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44389557-C-A

109441490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44389557-C-T

109441740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44389834-T-C

109441945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44390020-C-T

109442025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense variant
orthologous variants: 44390105-C-T

109442128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: synonymous variant
orthologous variants: 44390208-C-T

http://identifiers.org/hco/8/GRCh38#109442176-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44390256-A-C

109442194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 44390274-A-G

109442194-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 44390274-A-T

109442294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44390347-A-G

109442310-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44390372-T-A

109442310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44390372-T-C

109442376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44390437-A-G

http://identifiers.org/hco/8/GRCh38#109442396-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44390468-A-C

109442591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44390666-G-A

109442947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 44391015-T-C

109442947-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 44391015-T-G

109442955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense variant
orthologous variants: 44391023-C-T

http://identifiers.org/hco/8/GRCh38#109443061-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44391129-C-A

109443061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: synonymous variant
orthologous variants: 44391129-C-T

http://identifiers.org/hco/8/GRCh38#109443077-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44391145-C-A

109443077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense variant
orthologous variants: 44391145-C-T

109443262-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44391291-G-T

109443681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense variant
orthologous variants: 44391502-C-T

109443742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense variant
orthologous variants: 44391563-G-A

109443742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense variant
orthologous variants: 44391563-G-T

109443954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44391774-G-A

109443954-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44391774-G-C

http://identifiers.org/hco/8/GRCh38#109444008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44391824-C-A

109444156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44391975-C-T

109444552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44392350-T-C

109444590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44392382-G-T

http://identifiers.org/hco/8/GRCh38#109444597-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44392389-C-A

109444597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44392389-C-T

http://identifiers.org/hco/8/GRCh38#109444730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44392524-C-A

109444730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense variant
orthologous variants: 44392524-C-T

109444855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: synonymous variant
orthologous variants: 44392649-C-T

109444948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: synonymous variant
orthologous variants: 44392742-C-T

109445039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense variant
orthologous variants: 44392833-G-A

109445039-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense variant
orthologous variants: 44392833-G-T

http://identifiers.org/hco/8/GRCh38#109445063-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44392857-C-A

109445063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense variant
orthologous variants: 44392857-C-T

109445180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense variant
orthologous variants: 44392974-G-A

109445180-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense variant
orthologous variants: 44392974-G-T

http://identifiers.org/hco/8/GRCh38#109445227-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44393021-A-C

109445227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: synonymous variant
orthologous variants: 44393021-A-G

109445227-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense variant
orthologous variants: 44393021-A-T

109445282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense variant
orthologous variants: 44393076-C-T

109445512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: synonymous variant
orthologous variants: 44393306-C-T

109445740-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44393529-T-A

109445998-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44393777-T-A

109447704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44395706-A-G

109447758-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44395757-A-T

109447902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44395846-G-A

109447902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44395846-G-T

http://identifiers.org/hco/8/GRCh38#109448002-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44395946-C-A

109448002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44395946-C-T

109448038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44396018-A-G

109448045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44396147-G-A

109448267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 44396377-C-T

109448327-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 44396437-C-G

109448327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 44396437-C-T

http://identifiers.org/hco/8/GRCh38#109448431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44396526-C-A

109448732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44396586-C-T

109449294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44397093-T-C

109449333-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 44397134-A-T

109449343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense variant
orthologous variants: 44397144-T-C

109449366-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: synonymous variant
orthologous variants: 44397167-T-A

109449366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: synonymous variant
orthologous variants: 44397167-T-C

109449421-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense variant
orthologous variants: 44397222-G-C

109449421-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: stop gained
orthologous variants: 44397222-G-T

109449478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense variant
orthologous variants: 44397279-T-C

109449542-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44397346-G-T

109450014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44398051-A-G

109450226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44398259-T-C

http://identifiers.org/hco/8/GRCh38#109450234-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44398266-C-A

109450436-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44398612-T-G

109450539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44398714-C-T

109450549-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44398721-A-T

109450632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44398788-G-A

109450786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, undefined
orthologous variants: 44398924-T-C

109450788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, undefined
orthologous variants: 44398927-G-A

109450847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44398985-G-A

109450847-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44398985-G-T

109450896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, undefined
orthologous variants: 44399028-A-G

http://identifiers.org/hco/8/GRCh38#109450941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#44399073-C-A

109450941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, undefined
orthologous variants: 44399073-C-T

109450983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense_variant, undefined
orthologous variants: 44399118-G-A

http://identifiers.org/hco/8/GRCh38#109450984-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#44399119-C-A

http://identifiers.org/hco/8/GRCh38#109450993-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#44399128-C-A

109450993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense_variant, undefined
orthologous variants: 44399128-C-T

109451054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: synonymous_variant, undefined
orthologous variants: 44399189-C-T

109451063-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: synonymous_variant, undefined
orthologous variants: 44399198-A-T

http://identifiers.org/hco/8/GRCh38#109451162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#44399297-C-A

109451162-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, undefined
orthologous variants: 44399297-C-G

109451162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, undefined
orthologous variants: 44399297-C-T

http://identifiers.org/hco/8/GRCh38#109451222-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#44399355-C-A

109451222-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, undefined
orthologous variants: 44399355-C-G

109451222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, undefined
orthologous variants: 44399355-C-T

109451518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44399641-C-T

109451523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44399646-T-C

109451631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44399734-T-C

109451728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44399812-T-C

109452029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44400121-T-C

109452029-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44400121-T-G

109452046-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44400137-T-A

109452046-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44400137-T-G

109452101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44400184-T-C

109452138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense variant
orthologous variants: 44400219-A-G

109452138-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense variant
orthologous variants: 44400219-A-T

109452216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense variant
orthologous variants: 44400297-C-T

109452222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense variant
orthologous variants: 44400303-C-T

109452232-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: synonymous variant
orthologous variants: 44400313-G-T

109452237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense variant
orthologous variants: 44400318-C-T

http://identifiers.org/hco/8/GRCh38#109452312-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44400391-C-A

109452334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44400412-G-A

http://identifiers.org/hco/8/GRCh38#109452342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44400420-C-A

109452342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44400420-C-T

109452371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44400449-G-A

109452371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44400449-G-T

http://identifiers.org/hco/8/GRCh38#109452399-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44400476-C-A

109452400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44400477-A-G

109452525-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44400591-G-T

109452693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44400707-T-C

109452706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44400720-G-A

109452706-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44400720-G-T

http://identifiers.org/hco/8/GRCh38#109452715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44400729-C-A

109452715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 44400729-C-T

http://identifiers.org/hco/8/GRCh38#109452776-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44400790-A-C

109452776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense variant
orthologous variants: 44400790-A-G

109452776-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense variant
orthologous variants: 44400790-A-T

109452804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: synonymous variant
orthologous variants: 44400818-T-C

109452855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: synonymous variant
orthologous variants: 44400869-G-A

109452855-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense variant
orthologous variants: 44400869-G-C

109452855-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense variant
orthologous variants: 44400869-G-T

109452881-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 44400895-T-A

109452881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 44400895-T-C

109452890-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44400904-T-A

109452890-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44400904-T-C

109453262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44401174-G-A

109453262-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44401174-G-T

http://identifiers.org/hco/8/GRCh38#109453480-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44401797-A-C

http://identifiers.org/hco/8/GRCh38#109453669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44401971-C-A

109454193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense variant
orthologous variants: 44402317-G-A

http://identifiers.org/hco/8/GRCh38#109454252-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44402376-C-A

109454252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44402376-C-T

109454327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44402433-T-C

http://identifiers.org/hco/8/GRCh38#109454333-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44402439-A-C

109454333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44402439-A-G

109454333-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44402439-A-T

109454526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44402791-C-T

109454703-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44403023-A-T

109454743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: synonymous variant
orthologous variants: 44403061-A-G

109454743-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: synonymous variant
orthologous variants: 44403061-A-T

109455502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44403585-T-C

109455809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44403891-A-G

109456119-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44404114-T-G

109456128-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44404123-A-T

109456164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44404158-A-G

109456268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense variant
orthologous variants: 44404250-C-T

109456269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: synonymous variant
orthologous variants: 44404251-T-C

109456287-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: synonymous variant
orthologous variants: 44404269-T-A

109456302-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: synonymous variant
orthologous variants: 44404284-T-G

109456347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: synonymous variant
orthologous variants: 44404329-A-G

http://identifiers.org/hco/8/GRCh38#109456441-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44404413-A-C

109456441-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44404413-A-T

http://identifiers.org/hco/8/GRCh38#109456531-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44404718-A-C

109456616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44404806-G-A

109456779-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44404959-G-C

http://identifiers.org/hco/8/GRCh38#109456796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44404976-C-A

109456828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44405007-A-G

109456964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44405143-G-A

109457090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44405264-C-T

109457150-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44405320-G-C

109457150-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44405320-G-T

109457154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44405324-A-G

109459143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44406386-G-A

109459528-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44406720-T-A

109459528-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44406720-T-G

109459591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 44406762-A-G

109459634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: synonymous variant
orthologous variants: 44406805-T-C

109459712-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: synonymous variant
orthologous variants: 44406883-T-G

109459820-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: synonymous variant
orthologous variants: 44406991-T-A

109459887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44407057-A-G

109460121-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44407217-A-T

109460155-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44407254-T-G

109460427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44407504-T-C

109460930-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44408008-G-C

109460942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44408020-A-G

109461048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44408121-G-A

109461048-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44408121-G-T

109461135-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44408191-T-A

109461321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44408344-G-A

http://identifiers.org/hco/8/GRCh38#109461713-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44408696-C-A

109461713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44408696-C-T

109461719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44408702-T-C

109461743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44408724-T-C

http://identifiers.org/hco/8/GRCh38#109461842-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44408828-C-A

109461979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44408952-C-T

http://identifiers.org/hco/8/GRCh38#109461983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44408956-C-A

109461983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44408956-C-T

109462009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44408983-G-A

109462009-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44408983-G-C

109462009-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44408983-G-T

109464066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44409741-T-C

109464066-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44409741-T-G

109464111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44409785-T-C

109464198-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44409858-G-T

109464500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: synonymous variant
orthologous variants: 44410159-T-C

109464566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: synonymous variant
orthologous variants: 44410225-T-C

109464620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: synonymous variant
orthologous variants: 44410279-C-T

109464764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: synonymous variant
orthologous variants: 44410423-A-G

109464914-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: synonymous variant
orthologous variants: 44410573-A-T

109464931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense variant
orthologous variants: 44410590-A-G

109465004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: synonymous variant
orthologous variants: 44410663-A-G

http://identifiers.org/hco/8/GRCh38#109465022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44410681-C-A

109465022-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: synonymous variant
orthologous variants: 44410681-C-G

109465022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: synonymous variant
orthologous variants: 44410681-C-T

109465056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense variant
orthologous variants: 44410715-C-T

http://identifiers.org/hco/8/GRCh38#109465278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44411067-C-A

109465278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44411067-C-T

http://identifiers.org/hco/8/GRCh38#109465350-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44411159-C-A

109465350-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44411159-C-G

109465404-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44411257-T-A

109465450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44411303-C-T

109465505-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44411358-T-G

109465595-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44411434-A-T

109465697-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44411527-T-A

109465820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44413278-A-G

109465829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44413287-G-A

109465915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44413376-A-G

109465936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44413397-T-C

109465942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44413400-A-G

109465960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44413426-G-A

109466094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44413566-A-G

109466142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44413614-G-A

109466176-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44413642-T-A

109466176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44413642-T-C

109466253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44413798-G-A

109466262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44413807-G-A

http://identifiers.org/hco/8/GRCh38#109466322-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44413901-A-C

109466345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44413920-G-A

109466345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44413920-G-T

109466546-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44414113-T-A

109466588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: synonymous variant
orthologous variants: 44414155-A-G

109466751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense variant
orthologous variants: 44414318-G-A

109466784-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44414351-T-A

109466983-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44414545-G-C

109466985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44414547-A-G

109467059-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44414625-T-A

109467097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44414663-C-T

109467636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44407502-A-G

109467710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44415768-A-G

109467846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44415904-C-T

109467889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44415946-C-T

109467898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44415955-G-A

109467898-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44415955-G-T

109469368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44417051-G-A

109469496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44417169-A-G

109469506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44417179-C-T

109469528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44417200-A-G

109469550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44417219-G-A

109469598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44417260-T-C

109475063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, undefined
orthologous variants: 44417894-G-A

109475063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, undefined
orthologous variants: 44417894-G-T

109475065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, undefined
orthologous variants: 44417896-G-A

109475065-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, undefined
orthologous variants: 44417896-G-T

109475137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: synonymous variant
orthologous variants: 44417967-T-C

109476070-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44418873-T-G

109476251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44419026-A-G

109476422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44419201-T-C

109476437-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44419216-T-G

http://identifiers.org/hco/8/GRCh38#109476474-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44419255-C-A

109476474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44419255-C-T

109476495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44419279-T-C

109476528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense variant
orthologous variants: 44419311-A-G

109476528-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: synonymous variant
orthologous variants: 44419311-A-T

109476624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: synonymous variant
orthologous variants: 44419407-G-A

109476624-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: synonymous variant
orthologous variants: 44419407-G-T

109476636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: synonymous variant
orthologous variants: 44419419-T-C

109476747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44419526-T-C

109476772-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44419551-G-C

109476772-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44419551-G-T

109476792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44419571-G-A

http://identifiers.org/hco/8/GRCh38#109476802-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44419581-A-C

109476905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44419681-T-C

109477107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44420043-A-G

109477131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44420077-A-G

109477131-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44420077-A-T

http://identifiers.org/hco/8/GRCh38#109477133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44420079-C-A

109477133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44420079-C-T

http://identifiers.org/hco/8/GRCh38#109477148-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44420093-C-A

109477186-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44420131-T-G

109477212-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44420165-A-T

109477277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: synonymous variant
orthologous variants: 44420230-T-C

109477402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44420355-T-C

109477497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44420368-A-G

109477560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44420433-C-T

109477623-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44420496-C-G

109479385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44420930-A-G

109479426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44420971-G-A

109479426-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44420971-G-T

109479459-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44421004-T-G

http://identifiers.org/hco/8/GRCh38#109479511-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44421282-C-A

109479511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44421282-C-T

109479610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense variant
orthologous variants: 44421379-A-G

109479679-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44421447-T-A

109479679-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44421447-T-G

109479714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44421482-G-A

109479714-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44421482-G-T

109479751-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44421539-A-T

109479763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44421551-T-C

109479769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44421557-T-C

http://identifiers.org/hco/8/GRCh38#109479840-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44421771-C-A

http://identifiers.org/hco/8/GRCh38#109479900-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44421821-A-C

109479900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44421821-A-G

109479956-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44421878-G-T

109479960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44421882-A-G

109479991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 44421907-G-A

109479991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 44421907-G-T

109480033-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense variant
orthologous variants: 44421949-G-T

http://identifiers.org/hco/8/GRCh38#109480134-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44422050-C-A

109480134-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense variant
orthologous variants: 44422050-C-G

109480134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: synonymous variant
orthologous variants: 44422050-C-T

http://identifiers.org/hco/8/GRCh38#109480202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44422119-C-A

http://identifiers.org/hco/8/GRCh38#109480226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44422142-C-A

109480226-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44422142-C-G

109480339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44422287-A-G

109480433-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44422378-G-T

http://identifiers.org/hco/8/GRCh38#109480631-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44422583-C-A

109480631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 44422583-C-T

109480668-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 44422616-C-G

109480669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 44422617-T-C

http://identifiers.org/hco/8/GRCh38#109480697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44422645-C-A

109480697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44422645-C-T

109480751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44423106-T-C

109480779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44423132-C-T

109481102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44423440-G-A

109481143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44423481-T-C

109481143-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44423481-T-G

109481231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44423573-T-C

109481329-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44423673-T-A

109481329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44423673-T-C

109481378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44423725-G-A

109481378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44423725-G-T

http://identifiers.org/hco/8/GRCh38#109481422-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44423773-C-A

109481422-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44423773-C-G

109481422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44423773-C-T

109481534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: synonymous variant
orthologous variants: 44423885-A-G

http://identifiers.org/hco/8/GRCh38#109481539-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44423890-C-A

109481558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: synonymous variant
orthologous variants: 44423909-C-T

109481696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44424003-A-G

109482950-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44425136-T-G

109482959-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44425145-T-A

109482959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44425145-T-C

109482959-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44425145-T-G

109483129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44425300-G-T

109483130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44425301-A-G

109483164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44425333-G-A

109483166-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44425335-T-A

109483231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44425393-G-A

109483231-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44425393-G-T

109484954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44425927-C-T

109484994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44425964-A-G

109485005-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44425975-T-A

http://identifiers.org/hco/8/GRCh38#109485088-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44426058-C-A

109485088-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense variant
orthologous variants: 44426058-C-G

109485094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: synonymous variant
orthologous variants: 44426064-A-G

109486203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44427261-G-A

109486253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44427308-G-A

109486253-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44427308-G-C

http://identifiers.org/hco/8/GRCh38#109486532-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44427537-C-A

109486532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44427537-C-T

109486558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44427563-G-T

http://identifiers.org/hco/8/GRCh38#109486614-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44427617-C-A

109486614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44427617-C-T

109486627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44427630-C-T

109486740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense variant
orthologous variants: 44427740-G-A

109486748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: synonymous variant
orthologous variants: 44427748-C-T

109486774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense variant
orthologous variants: 44427774-C-T

109487173-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44428115-G-T

109489499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44429192-A-G

109489527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44429223-C-T

http://identifiers.org/hco/8/GRCh38#109489538-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44429234-A-C

109489832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44429549-A-G

109489832-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44429549-A-T

109490073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44429785-A-G

http://identifiers.org/hco/8/GRCh38#109490161-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44430341-C-A

109490161-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44430341-C-G

109490399-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44430649-A-T

109490744-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44431422-G-T

http://identifiers.org/hco/8/GRCh38#109490754-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44431432-A-C

http://identifiers.org/hco/8/GRCh38#109490899-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44431557-C-A

109490899-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44431557-C-G

109490901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44431559-T-C

109490905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44431563-C-T

109490974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 44431631-T-C

109491000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense variant
orthologous variants: 44431657-G-A

109491000-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense variant
orthologous variants: 44431657-G-C

109491058-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: synonymous variant
orthologous variants: 44431715-A-T

109491108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 44431765-T-C

109491120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44431777-G-A

109491120-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44431777-G-C

109491120-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44431777-G-T

109491147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44431796-T-C

109491161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44431809-A-G

109491162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44431810-C-T

http://identifiers.org/hco/8/GRCh38#109491180-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44431828-C-A

109491180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44431828-C-T

109491487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44432499-T-C

109491518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44432546-A-G

109491585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44432611-T-C

109491707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44432722-T-C

109491752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44432750-G-A

http://identifiers.org/hco/8/GRCh38#109491796-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44432791-A-C

109491796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44432791-A-G

http://identifiers.org/hco/8/GRCh38#109491797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44432792-C-A

109491797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44432792-C-T

109491800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44432795-T-C

http://identifiers.org/hco/8/GRCh38#109491804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44432799-C-A

109491804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44432799-C-T

http://identifiers.org/hco/8/GRCh38#109491859-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44432837-C-A

109491859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44432837-C-T

109492007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44432992-A-G

109492028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44433042-A-G

109492028-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44433042-A-T

109492094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44433110-A-G

109492094-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44433110-A-T

109493517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44433244-G-A

109493520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44433247-A-G

109493520-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44433247-A-T

109493556-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44433253-T-A

109493598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44433296-T-C

109493609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44433305-A-G

109493609-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44433305-A-T

109493618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44433314-T-C

109493630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44433326-G-A

109493630-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44433326-G-C

109493630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44433326-G-T

109493654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 44433348-G-A

109493654-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 44433348-G-C

109493654-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 44433348-G-T

109493744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: synonymous variant
orthologous variants: 44433438-T-C

109493840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44433532-A-G

http://identifiers.org/hco/8/GRCh38#109493849-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44433541-C-A

http://identifiers.org/hco/8/GRCh38#109493864-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44433556-A-C

109493864-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44433556-A-T

109493884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44433568-T-C

109494014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44433881-G-A

109494094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44433968-T-C

109494207-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44434070-G-T

109494274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44434137-A-G

109494403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44434248-T-C

109494486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44434609-C-T

109494531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44434655-G-A

109494598-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44434707-A-T

109494789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44434891-C-T

109495051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44435383-C-T

109495489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44436045-T-C

109495558-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44436091-A-T

109495743-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44436245-A-T

109497154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense variant
orthologous variants: 44437204-C-T

109497164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: synonymous variant
orthologous variants: 44437214-G-A

109497282-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44437332-T-G

http://identifiers.org/hco/8/GRCh38#109497329-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44437367-A-C

109497336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44437374-A-G

109497336-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44437374-A-T

http://identifiers.org/hco/8/GRCh38#109497372-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44437425-C-A

109497392-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44437445-T-A

109498436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44437779-A-G

109498436-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44437779-A-T

109498443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44437786-T-C

109498569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 44437910-A-G

109498610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44437950-G-A

109498725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 44438065-A-G

109498743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 44438083-T-C

109498897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 44438239-A-G

http://identifiers.org/hco/8/GRCh38#109498908-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44438264-A-C

http://identifiers.org/hco/8/GRCh38#109498923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44438279-C-A

109498929-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 44438285-T-G

109498933-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 44438289-A-T

http://identifiers.org/hco/8/GRCh38#109503420-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44441043-C-A

109503420-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44441043-C-G

http://identifiers.org/hco/8/GRCh38#109503819-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44441405-C-A

109503848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44441431-G-A

109503955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44441536-G-A

109504050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44441628-A-G

109504100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44441682-C-T

109504178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44441745-A-G

109504222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44441789-T-C

109504222-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44441789-T-G

109504228-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44441795-A-G

109504235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44441802-G-A

http://identifiers.org/hco/8/GRCh38#109504237-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44441804-C-A

109504237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44441804-C-T

http://identifiers.org/hco/8/GRCh38#109504282-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44441842-C-A

109504282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44441842-C-T

109504442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: synonymous variant
orthologous variants: 44442003-G-A

http://identifiers.org/hco/8/GRCh38#109504543-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44442098-C-A

109504543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44442098-C-T

109504674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44442214-T-C

http://identifiers.org/hco/8/GRCh38#109505233-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44442488-A-C

109505478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44442719-C-T

109505586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44442814-G-A

http://identifiers.org/hco/8/GRCh38#109505987-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44442906-C-A

109506194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44443107-G-A

109506228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, undefined
orthologous variants: 44443144-C-T

109506245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44443161-G-A

109506266-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44443182-G-C

109506283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, undefined
orthologous variants: 44443188-T-C

109506308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, undefined
orthologous variants: 44443209-G-A

109506319-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, undefined
orthologous variants: 44443224-T-G

109506441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44443329-A-G

109506441-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44443329-A-T

109506772-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44444329-T-A

109506830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44444407-G-A

109507177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44444731-C-T

109507641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44445094-A-G

109507801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: synonymous variant
orthologous variants: 44445259-C-T

109507907-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44445365-C-G

http://identifiers.org/hco/8/GRCh38#109507938-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44445392-A-C

109507938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44445392-A-G

109507950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44445404-A-G

109507952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44445406-G-A

109508007-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44445458-A-T

109508088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44445535-T-C

109508288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44445735-T-C

109508350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44445791-C-T

109508385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44445825-T-C

http://identifiers.org/hco/8/GRCh38#109508386-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44445826-C-A

109508386-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44445826-C-G

109508406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44445846-T-C

109508626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44446077-A-G

109508851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44446305-G-A

109508888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44446342-A-G

109508888-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44446342-A-T

109509353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44446773-G-T

109509408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44446829-C-T

109509741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44447132-G-A

109509741-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44447132-G-C

109510018-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44447378-G-C

109510055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44447415-G-A

109510553-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44447977-A-T

109510557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44447982-G-T

109510639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44448064-A-G

109510644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44448069-T-C

109510644-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44448069-T-G

109510724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44448163-A-G

109510733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44448172-A-G

109510832-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: synonymous variant
orthologous variants: 44448270-G-C

109510954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44448401-G-T

http://identifiers.org/hco/8/GRCh38#109510991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44448431-C-A

109510991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44448431-C-T

109511130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44448554-A-G

109511151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44448564-G-A

109513345-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44448657-A-T

109513380-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44448701-C-G

109513381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44448702-T-C

109513391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44448712-A-G

109513484-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44448806-T-G

109513872-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44449197-A-T

109515342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44449957-T-C

109515342-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44449957-T-G

109516657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44451505-A-G

109516719-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44451550-T-A

109517295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44451904-A-G

109517854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44452476-G-A

http://identifiers.org/hco/8/GRCh38#109518008-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44452615-A-C

109518625-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44453213-G-T

109520173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44453455-C-T

109520239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44453517-G-A

109520241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44453519-C-T

109520285-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44453586-T-A

109520612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44453762-C-T

109520699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44453846-T-C

109520849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44454027-T-C

109521052-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44454193-G-C

109521061-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44454202-G-C

109521189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44454317-G-A

109521379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44454473-A-G

109521415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44454535-G-A

109521541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44454642-T-C

109521547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44454648-G-A

109521673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44454769-T-C

109521765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44454859-A-G

109522163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44455245-T-C

109522177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44455260-T-C

http://identifiers.org/hco/8/GRCh38#109522233-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44455316-C-A

http://identifiers.org/hco/8/GRCh38#109522349-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44455432-C-A

109522349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44455432-C-T

109522412-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44456927-C-G

109522412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44456927-C-T

109522779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: synonymous variant
orthologous variants: 44457888-T-C

109522789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense variant
orthologous variants: 44457898-G-A

109522789-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense variant
orthologous variants: 44457898-G-T

109522971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44458039-G-A

109522971-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44458039-G-C

109523008-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44458062-G-T

109523040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44458098-G-A

109523040-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44458098-G-C

109523092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44458153-G-A

109523170-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44458221-A-T

http://identifiers.org/hco/8/GRCh38#109523188-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44458239-A-C

109523188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44458239-A-G

109523201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44458251-G-T

109523230-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 44458280-T-A

109523230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 44458280-T-C

109523241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 44458291-T-C

109523241-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44458291-T-G

109523394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 44458444-C-T

109523442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44458692-A-G

http://identifiers.org/hco/8/GRCh38#109526679-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44460177-C-A

109526720-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44460223-G-T

109526726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44460229-G-A

109526825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44460315-G-A

http://identifiers.org/hco/8/GRCh38#109526833-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44460323-A-C

109526942-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44460453-G-C

109526950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 44460461-C-T

109526972-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44460483-C-G

109526972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44460483-C-T

109527011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44460522-A-G

http://identifiers.org/hco/8/GRCh38#109527015-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44460526-C-A

109527015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44460526-C-T

109527048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44460563-T-C

http://identifiers.org/hco/8/GRCh38#109527087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44460618-C-A

109527187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44460716-T-C

http://identifiers.org/hco/8/GRCh38#109527190-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44460719-A-C

109527190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44460719-A-G

109527448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44460821-G-A

109527615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44460833-G-A

109528038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44461180-G-A

109528061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44461203-T-C

109528101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44461243-A-G

109528804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44462385-C-T

109528805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44462386-G-A

109528832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44462413-T-C

109528992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44462563-A-G

109529144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44462664-T-C

109529753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron variant
orthologous variants: 44463749-C-T

109530083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, missense_variant
orthologous variants: 44464559-G-A

109530083-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, missense_variant
orthologous variants: 44464559-G-C

109530083-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: intron_variant, missense_variant
orthologous variants: 44464559-G-T

109530091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 44464567-A-G

109530091-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 44464567-A-T

http://identifiers.org/hco/8/GRCh38#109530100-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44464576-C-A

109530100-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 44464576-C-G

109530100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 44464576-C-T

109530125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 44464601-A-G

109530125-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 44464601-A-T

109530129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 44464605-G-A

109530129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 44464605-G-T

http://identifiers.org/hco/8/GRCh38#109530156-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44464640-A-C

109530156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 44464640-A-G

109530169-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 44464654-T-A

109530169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 44464654-T-C

109530191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 44464676-T-C

http://identifiers.org/hco/8/GRCh38#109530329-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44464815-C-A

109530357-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 44464843-G-T

109530501-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 44465051-T-G

109530525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 44465076-A-G

109530597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 44465120-C-T

109530753-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: 3 prime UTR variant
orthologous variants: 44465236-C-G

109530753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: 3 prime UTR variant
orthologous variants: 44465236-C-T

109530761-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: 3 prime UTR variant
orthologous variants: 44465244-C-G

109530767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: 3 prime UTR variant
orthologous variants: 44465250-C-T

109531042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: 3 prime UTR variant
orthologous variants: 44465442-G-A

http://identifiers.org/hco/8/GRCh38#109531631-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#44466320-A-C

109531866-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: 3 prime UTR variant
orthologous variants: 44466544-G-C

109531889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: 3 prime UTR variant
orthologous variants: 44466568-C-T

109532295-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: 3 prime UTR variant
orthologous variants: 44466910-G-T

109534571-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: 3 prime UTR variant
orthologous variants: 44476073-G-T

109534753-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: 3 prime UTR variant
orthologous variants: 44476258-G-C

109534847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: 3 prime UTR variant
orthologous variants: 44476309-G-A

109534847-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: 3 prime UTR variant
orthologous variants: 44476309-G-C

109535185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: 3 prime UTR variant
orthologous variants: 44476622-G-A

109535192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: 3 prime UTR variant
orthologous variants: 44476629-G-A

109535617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: 3 prime UTR variant
orthologous variants: 44477026-C-T

109535766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: 3 prime UTR variant
orthologous variants: 44477186-C-T

109535797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: 3 prime UTR variant
orthologous variants: 44477206-T-C

109535910-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: 3 prime UTR variant
orthologous variants: 44477296-G-C

109536385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: 3 prime UTR variant
orthologous variants: 44477943-T-C

109536403-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: 3 prime UTR variant
orthologous variants: 44477959-T-G

109536869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: 3 prime UTR variant
orthologous variants: 44478395-G-A

109536869-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: 3 prime UTR variant
orthologous variants: 44478395-G-T

109537066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20313
most severe consequence: 3 prime UTR variant
orthologous variants: 44479582-T-C