80101569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 119158876-C-T

http://identifiers.org/hco/17/GRCh38#80101801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119159108-C-A

80101801-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119159108-C-G

80101801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119159108-C-T

80101831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 119159140-G-A

80101831-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 119159140-G-T

80101915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 119159223-C-T

http://identifiers.org/hco/17/GRCh38#80104518-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119160876-C-A

80104518-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119160876-C-G

80104518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119160876-C-T

80104529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119160887-G-A

80104529-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119160887-G-T

80104673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 119161045-C-T

80104682-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 119161054-C-G

80104712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 119161084-G-A

80104712-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 119161084-G-C

80104725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 119161097-C-T

80104742-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 119161114-T-A

80104747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 119161119-C-T

80104753-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 119161125-A-T

80104784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 119161156-G-A

80104790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 119161162-C-T

80104798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 119161170-A-G

80104885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 119161257-A-G

http://identifiers.org/hco/17/GRCh38#80104904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119161276-C-A

80104904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 119161276-C-T

http://identifiers.org/hco/17/GRCh38#80104946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119161318-C-A

http://identifiers.org/hco/17/GRCh38#80105149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119161561-C-A

80105149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119161561-C-T

http://identifiers.org/hco/17/GRCh38#80105158-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119161587-C-A

80105158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119161587-C-T

http://identifiers.org/hco/17/GRCh38#80105176-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119161604-C-A

80105176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119161604-C-T

80105222-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119161645-T-A

80105254-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119161676-G-T

80105259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119161681-G-A

80105760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 119163707-A-G

80105802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 119163749-C-T

80107544-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119164789-C-G

80107544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119164789-C-T

80107596-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 119164840-G-C

80107740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119164983-G-A

80107778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119165020-C-T

80107928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119165165-G-A

80107947-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119165191-T-A

80107976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119165218-G-A

80107976-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119165218-G-T

80108141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119165328-G-A

80108141-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119165328-G-T

http://identifiers.org/hco/17/GRCh38#80108206-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119165403-C-A

80108206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119165403-C-T

80108276-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119165457-T-A

80108276-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119165457-T-G

80108283-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 119165460-C-G

80108366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 119165543-C-T

80108443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119165619-C-T

80108455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119165631-C-T

80108473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119165666-C-T

80108520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 119165713-G-A

80108520-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 119165713-G-C

80108520-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 119165713-G-T

80108604-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 119165797-C-G

80108604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 119165797-C-T

80108632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119165825-G-A

80108632-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119165825-G-C

80108650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119165840-A-G

80108680-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119165870-C-G

80108681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119165871-C-T

80108699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 119165888-C-T

80108788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 119165977-A-G

80108803-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 119165992-G-C

80108803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 119165992-G-T

80108857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119166031-G-A

80108857-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119166031-G-C

80108857-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119166031-G-T

80108859-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119166033-A-T

80108860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119166034-A-G

80108880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119166041-G-A

80108880-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119166041-G-C

http://identifiers.org/hco/17/GRCh38#80108900-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119166061-C-A

80108900-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119166061-C-G

80108900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119166061-C-T

80109908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119167632-G-A

80109908-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119167632-G-C

80109933-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119167658-C-G

80109933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119167658-C-T

80109992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 119167715-C-T

80110013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 119167736-G-A

http://identifiers.org/hco/17/GRCh38#80110028-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119167751-C-A

80110028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 119167751-C-T

80110064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119167785-A-G

80110077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119167792-C-T

80110078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119167793-G-A

80110207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119167836-G-A

80110320-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119167957-G-T

80110396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119168054-G-A

80110484-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119168119-C-G

80110623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119168226-A-G

80110623-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119168226-A-T

80110625-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119168228-T-A

80110625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119168228-T-C

80110643-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119168246-T-A

80110643-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119168246-T-G

http://identifiers.org/hco/17/GRCh38#80110644-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119168247-C-A

80110644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119168247-C-T

http://identifiers.org/hco/17/GRCh38#80110693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119168298-C-A

80110735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 119168335-C-T

80110753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 119168353-C-T

80111065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119168660-T-C

80111680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119168830-G-A

80111680-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119168830-G-T

http://identifiers.org/hco/17/GRCh38#80111742-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119168884-C-A

80111746-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 119168887-A-G

80111747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 119168888-G-T

http://identifiers.org/hco/17/GRCh38#80111751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119168892-C-A

80111752-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 119168893-C-G

80111752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 119168893-C-T

80111830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 119168933-C-T

http://identifiers.org/hco/17/GRCh38#80111845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119168945-C-A

80111845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 119168945-C-T

http://identifiers.org/hco/17/GRCh38#80111848-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119168948-C-A

80111880-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 119168972-G-T

http://identifiers.org/hco/17/GRCh38#80111900-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119168990-C-A

80111900-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 119168990-C-G

80111900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 119168990-C-T

80112133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119169230-C-T

http://identifiers.org/hco/17/GRCh38#80112134-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119169231-C-A

80112152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119169249-A-G

http://identifiers.org/hco/17/GRCh38#80112174-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119169292-C-A

80112174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119169292-C-T

80112175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119169293-T-C

80112196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119169314-G-A

80112196-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119169314-G-T

80112210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119169328-G-A

80112210-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119169328-G-C

80112210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119169328-G-T

80112213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119169331-G-A

80112213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119169331-G-T

80112232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119169352-G-A

80112232-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119169352-G-T

http://identifiers.org/hco/17/GRCh38#80112240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119169370-C-A

80112240-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119169370-C-G

80112240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119169370-C-T

80112248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119169377-G-A

80112248-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119169377-G-C

80112248-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119169377-G-T

80112269-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119169398-T-A

80112269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119169398-T-C

80112286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119169411-C-T

80112318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119169428-T-C

80112371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119169478-G-A

80112371-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119169478-G-C

80112371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119169478-G-T

80112388-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119169492-A-T

80112424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119169532-G-A

80112424-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119169532-G-T

http://identifiers.org/hco/17/GRCh38#80112468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119169570-C-A

80112473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119169575-G-A

80112473-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119169575-G-T

80112476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119169578-T-C

80112519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119169629-A-G

80112729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119169843-G-A

80112729-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119169843-G-C

80112763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119169873-A-G

80112770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119169880-G-A

http://identifiers.org/hco/17/GRCh38#80112775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119169888-C-A

80112775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119169888-C-T

80112802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119169910-G-A

http://identifiers.org/hco/17/GRCh38#80112833-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119171198-C-A

80112833-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119171198-C-G

80113035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 119171397-G-A

80113035-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 119171397-G-C

80113035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 119171397-G-T

http://identifiers.org/hco/17/GRCh38#80113078-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119171427-C-A

80113078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119171427-C-T

80113132-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119171497-A-T

80113189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119171910-T-C

http://identifiers.org/hco/17/GRCh38#80113191-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119171912-C-A

80113191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119171912-C-T

http://identifiers.org/hco/17/GRCh38#80113194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119171915-C-A

80113194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119171915-C-T

80113229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 119171950-G-A

80113229-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 119171950-G-C

80113229-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 119171950-G-T

http://identifiers.org/hco/17/GRCh38#80113241-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119171962-C-A

80113241-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 119171962-C-G

80113241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 119171962-C-T

80113247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 119171968-G-A

80113247-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 119171968-G-C

80113247-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 119171968-G-T

http://identifiers.org/hco/17/GRCh38#80113272-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119171993-C-A

80113272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 119171993-C-T

80113383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119172104-G-A

80113383-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119172104-G-T

http://identifiers.org/hco/17/GRCh38#80113395-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119172118-C-A

80113395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119172118-C-T

80113421-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119172154-T-A

80113421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119172154-T-C

80113422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119172155-A-G

http://identifiers.org/hco/17/GRCh38#80113428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119172161-C-A

80113428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119172161-C-T

http://identifiers.org/hco/17/GRCh38#80113437-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119172170-C-A

80113437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119172170-C-T

80117070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 119174102-T-C

80117107-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 119174139-A-T

80117201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119174171-G-A

80117201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119174171-G-T

http://identifiers.org/hco/17/GRCh38#80117239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119174191-C-A

80117239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119174191-C-T

http://identifiers.org/hco/17/GRCh38#80117457-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119174342-C-A

80117457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119174342-C-T

http://identifiers.org/hco/17/GRCh38#80117477-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119174357-C-A

80117477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119174357-C-T

80117489-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119174369-A-T

80117572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119174456-G-A

80117646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 119174534-C-T

http://identifiers.org/hco/17/GRCh38#80117759-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119174648-C-A

80117759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119174648-C-T

80117806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119174682-G-A

80117806-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119174682-G-T

80117817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119174691-A-G

80117817-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119174691-A-T

80117819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119174693-A-G

80117827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119174701-G-A

80117827-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119174701-G-T

80117828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119174702-G-A

80117885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119174708-G-T

80117889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119174712-G-A

80117889-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119174712-G-T

80117913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119174720-C-T

80118109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119174835-T-C

http://identifiers.org/hco/17/GRCh38#80118111-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119174837-C-A

80118111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119174837-C-T

http://identifiers.org/hco/17/GRCh38#80118190-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119174882-C-A

80118190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 119174882-C-T

80118306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 119174998-G-A

http://identifiers.org/hco/17/GRCh38#80118309-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119175001-A-C

80118309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 119175001-A-G

80118384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119175077-T-C

http://identifiers.org/hco/17/GRCh38#80118557-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119175195-C-A

80118557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119175195-C-T

80118773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 119175393-G-A

80118773-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 119175393-G-T

80118796-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 119175416-C-G

80118796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 119175416-C-T

80118831-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119175451-G-T

80118860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119175465-G-A

80118860-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119175465-G-T

80118902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119175526-A-G

80118968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119175565-G-A

80118983-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119175581-G-C

80118983-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119175581-G-T

80119078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119175659-A-G

80119292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 119175851-G-A

80119292-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 119175851-G-C

80119292-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 119175851-G-T

80119345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 119175895-G-A

80119410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 119175937-G-A

80119410-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 119175937-G-T

80119523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 119175996-G-A

80119523-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 119175996-G-T

80119548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 119176017-G-A

http://identifiers.org/hco/17/GRCh38#80119559-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119176028-C-A

80119559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 119176028-C-T

http://identifiers.org/hco/17/GRCh38#80119644-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119176077-C-A

80119644-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 119176077-C-G

80119683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 119176126-G-A

80119683-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 119176126-G-C

http://identifiers.org/hco/17/GRCh38#80119746-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#119176175-C-A

80119746-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 119176175-C-G

80119746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 119176175-C-T

80119782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 119176204-G-A

80119827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4065
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 119176227-G-A