http://identifiers.org/hco/16/GRCh38#4958358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#4964860-C-A

4958358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 4964860-C-T

4958454-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 4964939-C-G

http://identifiers.org/hco/16/GRCh38#4958457-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#4964942-C-A

4958457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 4964942-C-T

http://identifiers.org/hco/16/GRCh38#4958461-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#4964946-C-A

4958461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 4964946-C-T

http://identifiers.org/hco/16/GRCh38#4958462-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#4964947-C-A

4958462-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 4964947-C-G

http://identifiers.org/hco/16/GRCh38#4958487-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#4964978-C-A

4958487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 4964978-C-T

4958532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 4965016-T-C

http://identifiers.org/hco/16/GRCh38#4958595-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#4965071-C-A

4958595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4965071-C-T

http://identifiers.org/hco/16/GRCh38#4958805-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#4965212-C-A

4958814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4965221-G-A

4959048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4965431-G-A

4959051-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4965434-C-G

4959051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4965434-C-T

4959147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4965519-G-T

http://identifiers.org/hco/16/GRCh38#4959245-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#4965580-C-A

4959245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4965580-C-T

http://identifiers.org/hco/16/GRCh38#4959263-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#4965598-C-A

4959263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 4965598-C-T

http://identifiers.org/hco/16/GRCh38#4959283-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#4965619-C-A

4959283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 4965619-C-T

4959332-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron_variant, missense_variant
orthologous variants: 4965658-A-T

4959375-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron_variant, missense_variant
orthologous variants: 4965701-C-G

4962423-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4967952-C-G

4962466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4967993-C-T

4962558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4968138-A-G

4962591-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4968177-G-C

4962665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4968342-G-A

http://identifiers.org/hco/16/GRCh38#4962693-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#4968371-A-C

http://identifiers.org/hco/16/GRCh38#4962700-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#4968384-A-C

http://identifiers.org/hco/16/GRCh38#4962704-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#4968388-A-C

4962704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4968388-A-G

4962704-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4968388-A-T

4962867-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4968548-C-G

4968667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4971364-C-T

4968723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4971418-G-A

4969174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4971797-G-A

4976567-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4974794-C-G

4976567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4974794-C-T

4976589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4974816-G-A

4976592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4974819-A-G

4976592-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4974819-A-T

4976943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4975190-T-C

4976961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4975208-A-G

4977018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4975272-G-A

4977018-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4975272-G-T

4977284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4975618-T-C

http://identifiers.org/hco/16/GRCh38#4977444-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#4975837-C-A

4977486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4975879-G-A

http://identifiers.org/hco/16/GRCh38#4977533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#4975920-C-A

4982310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4980397-C-T

4982323-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4980410-C-G

4982323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4980410-C-T

4982438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4980444-G-A

4982479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4980483-G-A

4987586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: synonymous variant
orthologous variants: 4983482-A-G

4987630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: missense variant
orthologous variants: 4983526-G-A

4987630-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: missense variant
orthologous variants: 4983526-G-C

4987630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: missense variant
orthologous variants: 4983526-G-T

http://identifiers.org/hco/16/GRCh38#4987635-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#4983531-C-A

4987691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: synonymous variant
orthologous variants: 4983587-G-A

4987691-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: synonymous variant
orthologous variants: 4983587-G-C

4987691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: synonymous variant
orthologous variants: 4983587-G-T

4987719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4983611-G-A

4987719-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4983611-G-C

4987719-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4983611-G-T

4987768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4983652-G-A

4987768-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4983652-G-C

4987768-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4983652-G-T

4987857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4983719-G-A

4987898-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4983742-G-C

4988026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4984747-T-C

4988026-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4984747-T-G

4988071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4984778-G-A

4988071-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4984778-G-C

4988071-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4984778-G-T

4988133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4984848-G-A

4988133-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4984848-G-C

4988133-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4984848-G-T

4988210-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: missense variant
orthologous variants: 4984930-C-G

4988210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: missense variant
orthologous variants: 4984930-C-T

4988226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: synonymous variant
orthologous variants: 4984946-G-A

4988226-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: synonymous variant
orthologous variants: 4984946-G-T

4988286-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4985006-C-G

4988286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4985006-C-T

http://identifiers.org/hco/16/GRCh38#4990687-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#4985662-C-A

4990687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4985662-C-T

4990718-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4985690-G-C

4990718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4985690-G-T

4990722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4985694-G-A

4990722-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4985694-G-T

4990733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4985705-T-C

4990733-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4985705-T-G

4990740-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4985712-C-G

4990740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4985712-C-T

4990825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: missense variant
orthologous variants: 4985797-G-A

4990825-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: missense variant
orthologous variants: 4985797-G-T

http://identifiers.org/hco/16/GRCh38#4990862-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#4985834-C-A

4990862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: synonymous variant
orthologous variants: 4985834-C-T

4990992-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4985935-G-T

http://identifiers.org/hco/16/GRCh38#4991789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#4986650-C-A

4991789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4986650-C-T

4991921-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: synonymous variant
orthologous variants: 4986771-C-G

4991921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: synonymous variant
orthologous variants: 4986771-C-T

4991933-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: missense variant
orthologous variants: 4986783-T-A

4991933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: synonymous variant
orthologous variants: 4986783-T-C

4991956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: missense variant
orthologous variants: 4986806-G-A

4991956-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: missense variant
orthologous variants: 4986806-G-C

4991956-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: missense variant
orthologous variants: 4986806-G-T

http://identifiers.org/hco/16/GRCh38#4991966-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#4986816-C-A

4991966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: synonymous variant
orthologous variants: 4986816-C-T

4991975-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: missense variant
orthologous variants: 4986825-G-T

http://identifiers.org/hco/16/GRCh38#4992009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#4986859-C-A

4992009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: synonymous variant
orthologous variants: 4986859-C-T

4992025-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: missense variant
orthologous variants: 4986875-T-A

4992151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4986984-G-A

4992151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4986984-G-T

4996331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4989706-C-T

4996424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: synonymous variant
orthologous variants: 4989801-G-A

4996424-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: missense variant
orthologous variants: 4989801-G-C

4996424-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: missense variant
orthologous variants: 4989801-G-T

http://identifiers.org/hco/16/GRCh38#4996494-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#4989883-A-C

4996504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4989893-G-A

4996504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4989893-G-T

4996808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4990795-G-A

4996808-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4990795-G-C

4996808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4990795-G-T

4996996-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: missense variant
orthologous variants: 4990982-G-T

http://identifiers.org/hco/16/GRCh38#5000641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#4993899-C-A

5000641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4993899-C-T

5000779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4994021-G-A

5000779-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4994021-G-T

5000820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4994056-G-A

5000869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: synonymous variant
orthologous variants: 4994105-C-T

5000896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: synonymous variant
orthologous variants: 4994132-G-A

5000896-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: synonymous variant
orthologous variants: 4994132-G-C

5000896-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: synonymous variant
orthologous variants: 4994132-G-T

5000910-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: missense variant
orthologous variants: 4994146-T-A

5000910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: missense variant
orthologous variants: 4994146-T-C

5000910-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: missense variant
orthologous variants: 4994146-T-G

http://identifiers.org/hco/16/GRCh38#5000923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#4994159-C-A

5000923-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 4994159-C-G

5000923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 4994159-C-T

5003368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4994282-G-A

5003368-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4994282-G-T

5003383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4994297-G-A

5003414-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: missense variant
orthologous variants: 4994350-C-G

5003414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: synonymous variant
orthologous variants: 4994350-C-T

5003423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: synonymous variant
orthologous variants: 4994359-C-T

5003432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: synonymous variant
orthologous variants: 4994368-A-G

5003534-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: missense variant
orthologous variants: 4994470-C-G

5003534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: synonymous variant
orthologous variants: 4994470-C-T

5005583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4995966-C-T

5005597-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4995981-C-G

5005597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4995981-C-T

5005601-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4995985-C-G

5005601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4995985-C-T

5005610-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4995994-C-G

5005649-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4996039-C-G

5005649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4996039-C-T

5005652-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4996057-G-C

5005666-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4996071-C-G

5005686-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4996092-C-G

5005686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4996092-C-T

5005703-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4996110-T-A

5005712-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4996119-A-T

5005754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4996143-C-T

5005945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: missense variant
orthologous variants: 4996389-G-A

5005945-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: missense variant
orthologous variants: 4996389-G-C

5005952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: synonymous variant
orthologous variants: 4996396-C-T

5005985-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: synonymous variant
orthologous variants: 4996429-C-G

5005985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: synonymous variant
orthologous variants: 4996429-C-T

5006054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4996498-G-A

5006161-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4996567-T-A

5006161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4996567-T-C

5006161-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4996567-T-G

5006174-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4996590-T-A

5006174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4996590-T-C

5006174-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4996590-T-G

http://identifiers.org/hco/16/GRCh38#5007082-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#4997816-C-A

5007314-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4998042-C-G

5007314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4998042-C-T

5008405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4998518-G-A

http://identifiers.org/hco/16/GRCh38#5008416-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#4998529-C-A

http://identifiers.org/hco/16/GRCh38#5008739-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#4998845-C-A

5008739-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4998845-C-G

5008739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4998845-C-T

5008743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4998849-G-A

5008743-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4998849-G-T

http://identifiers.org/hco/16/GRCh38#5008753-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#4998857-C-A

5008753-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4998857-C-G

5008753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4998857-C-T

5008783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4998884-A-G

5008783-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4998884-A-T

5010659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4999305-C-T

http://identifiers.org/hco/16/GRCh38#5010721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#4999358-C-A

5010721-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4999358-C-G

5010721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4999358-C-T

http://identifiers.org/hco/16/GRCh38#5010743-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#4999367-C-A

5010887-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4999451-G-T

5010919-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4999482-G-T

5010927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4999489-G-A

5010927-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4999489-G-T

5010928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4999490-G-A

5010928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4999490-G-T

http://identifiers.org/hco/16/GRCh38#5010929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#4999491-C-A

5010929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4999491-C-T

http://identifiers.org/hco/16/GRCh38#5010993-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#4999551-C-A

5010993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4999551-C-T

http://identifiers.org/hco/16/GRCh38#5011021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#4999579-C-A

5011021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 4999579-C-T

5011066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron_variant, undefined
orthologous variants: 4999623-G-A

5011066-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron_variant, undefined
orthologous variants: 4999623-G-T

5011193-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: missense variant
orthologous variants: 4999967-T-A

5011202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: synonymous variant
orthologous variants: 4999976-G-A

5011208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: synonymous variant
orthologous variants: 4999982-G-A

5011208-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: synonymous variant
orthologous variants: 4999982-G-C

5011700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 5000598-C-T

5011782-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 5000682-C-G

5011893-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 5000740-C-G

5014315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 5000983-G-A

5014433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 5001097-G-A

5014480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 5001133-T-C

5014563-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 5001242-G-C

5014615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 5001285-C-T

5014686-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 5001335-G-C

5014690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 5001339-G-A

5014690-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 5001339-G-C

http://identifiers.org/hco/16/GRCh38#5014711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#5001355-C-A

5014711-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 5001355-C-G

5014711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 5001355-C-T

5014738-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 5001382-T-G

5014764-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 5001438-G-T

5014828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: intron variant
orthologous variants: 5001473-G-A

5014970-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: undefined
orthologous variants: 5001614-G-T

http://identifiers.org/hco/16/GRCh38#5014998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#5001640-C-A

5014998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 3 prime UTR variant
orthologous variants: 5001640-C-T

5014999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 3 prime UTR variant
orthologous variants: 5001641-T-C

http://identifiers.org/hco/16/GRCh38#5015039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#5001681-C-A

5015039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 3 prime UTR variant
orthologous variants: 5001681-C-T

5015084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 3 prime UTR variant
orthologous variants: 5001719-G-A

5015084-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 3 prime UTR variant
orthologous variants: 5001719-G-C

5015085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 3 prime UTR variant
orthologous variants: 5001720-A-G

5015117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 3 prime UTR variant
orthologous variants: 5001752-G-A

5015117-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 3 prime UTR variant
orthologous variants: 5001752-G-T

5015153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 3 prime UTR variant
orthologous variants: 5001789-G-T

http://identifiers.org/hco/16/GRCh38#5015284-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#5001913-C-A

5015284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 3 prime UTR variant
orthologous variants: 5001913-C-T

http://identifiers.org/hco/16/GRCh38#5015325-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#5001968-A-C

5015325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 3 prime UTR variant
orthologous variants: 5001968-A-G

5015325-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 3 prime UTR variant
orthologous variants: 5001968-A-T

5015367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 3 prime UTR variant
orthologous variants: 5001997-G-A

5015367-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 3 prime UTR variant
orthologous variants: 5001997-G-C

5015367-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 3 prime UTR variant
orthologous variants: 5001997-G-T

http://identifiers.org/hco/16/GRCh38#5015384-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#5002014-C-A

5015384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 3 prime UTR variant
orthologous variants: 5002014-C-T

5015431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 3 prime UTR variant
orthologous variants: 5002054-A-G

http://identifiers.org/hco/16/GRCh38#5015536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#5002149-C-A

5015536-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 3 prime UTR variant
orthologous variants: 5002149-C-G

5015536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 3 prime UTR variant
orthologous variants: 5002149-C-T

http://identifiers.org/hco/16/GRCh38#5015588-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#5002175-C-A

5015588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 3 prime UTR variant
orthologous variants: 5002175-C-T

5015670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 3 prime UTR variant
orthologous variants: 5002236-A-G

5015673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 3 prime UTR variant
orthologous variants: 5002239-A-G

http://identifiers.org/hco/16/GRCh38#5015674-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#5002240-A-C

5015674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 3 prime UTR variant
orthologous variants: 5002240-A-G

5015726-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 3 prime UTR variant
orthologous variants: 5002278-T-A

5015862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 3 prime UTR variant
orthologous variants: 5002399-G-A

5015862-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 3 prime UTR variant
orthologous variants: 5002399-G-C

5015862-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 3 prime UTR variant
orthologous variants: 5002399-G-T

5015872-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 3 prime UTR variant
orthologous variants: 5002409-G-T

http://identifiers.org/hco/16/GRCh38#5015969-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#5002510-C-A

5015969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 3 prime UTR variant
orthologous variants: 5002510-C-T

5015975-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 3 prime UTR variant
orthologous variants: 5002516-G-C

5016076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 3 prime UTR variant
orthologous variants: 5002610-G-A

5016076-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 3 prime UTR variant
orthologous variants: 5002610-G-C

5016143-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 3 prime UTR variant
orthologous variants: 5002677-C-G

5016143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 3 prime UTR variant
orthologous variants: 5002677-C-T

5016158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 3 prime UTR variant
orthologous variants: 5002691-T-C

5016158-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 3 prime UTR variant
orthologous variants: 5002691-T-G

5016190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 3 prime UTR variant
orthologous variants: 5002722-G-A

5016377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 3 prime UTR variant
orthologous variants: 5002899-T-C

5016388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 3 prime UTR variant
orthologous variants: 5002923-G-A

5016388-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 3 prime UTR variant
orthologous variants: 5002923-G-T

5016411-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 3 prime UTR variant
orthologous variants: 5002946-T-A

5016486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 3 prime UTR variant
orthologous variants: 5002985-C-T

5016624-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 3 prime UTR variant
orthologous variants: 5003094-T-A

http://identifiers.org/hco/16/GRCh38#5016844-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#5003256-C-A

http://identifiers.org/hco/16/GRCh38#5016868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#5003281-C-A

5016903-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 3 prime UTR variant
orthologous variants: 5003319-G-T

5017036-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 3 prime UTR variant
orthologous variants: 5003441-G-T

http://identifiers.org/hco/16/GRCh38#5017430-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#5004049-C-A

http://identifiers.org/hco/16/GRCh38#5017491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#5004105-C-A

5017491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 3 prime UTR variant
orthologous variants: 5004105-C-T

http://identifiers.org/hco/16/GRCh38#5017515-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#5004126-A-C

5017515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 3 prime UTR variant
orthologous variants: 5004126-A-G

5017568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 3 prime UTR variant
orthologous variants: 5004181-G-T

5017582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 3 prime UTR variant
orthologous variants: 5004195-G-A

5017582-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 3 prime UTR variant
orthologous variants: 5004195-G-T

5017727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 3 prime UTR variant
orthologous variants: 5004406-A-G

5018005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 3 prime UTR variant
orthologous variants: 5004773-G-T

http://identifiers.org/hco/16/GRCh38#5018006-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#5004774-C-A

5018044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 3 prime UTR variant
orthologous variants: 5004795-T-C

5018064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 3 prime UTR variant
orthologous variants: 5004815-G-A

5018064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 3 prime UTR variant
orthologous variants: 5004815-G-T

5018091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 3 prime UTR variant
orthologous variants: 5004842-T-C

5018096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 3 prime UTR variant
orthologous variants: 5004847-T-C

5018847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 3 prime UTR variant
orthologous variants: 5005036-A-G

5018854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 3 prime UTR variant
orthologous variants: 5005043-A-G

5018855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 3 prime UTR variant
orthologous variants: 5005044-A-G

5018856-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 3 prime UTR variant
orthologous variants: 5005045-T-A

5018865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 3 prime UTR variant
orthologous variants: 5005054-T-C

5018890-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 3 prime UTR variant
orthologous variants: 5005068-T-A

5019003-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29032
most severe consequence: 3 prime UTR variant
orthologous variants: 5005167-G-T