http://identifiers.org/hco/17/GRCh38#9822229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67665268-C-A

9822241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 5 prime UTR variant
orthologous variants: 67665256-G-A

9822276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 5 prime UTR variant
orthologous variants: 67665214-T-C

http://identifiers.org/hco/17/GRCh38#9822279-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67665211-C-A

9822282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 5 prime UTR variant
orthologous variants: 67665208-G-A

9822282-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 5 prime UTR variant
orthologous variants: 67665208-G-T

9824457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67663406-T-C

9824506-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67663361-G-T

9824537-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67663298-G-T

9824557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67663278-C-T

9824835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67662990-A-G

9824881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67662945-T-C

9824971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67662871-G-A

9825375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67662463-G-A

http://identifiers.org/hco/17/GRCh38#9825418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67662401-C-A

9825418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67662401-C-T

http://identifiers.org/hco/17/GRCh38#9825432-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67662387-A-C

9825432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67662387-A-G

9825535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67662282-G-A

9825535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67662282-G-T

http://identifiers.org/hco/17/GRCh38#9825542-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67662276-C-A

9825542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67662276-C-T

http://identifiers.org/hco/17/GRCh38#9825583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67662239-C-A

9825600-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67662222-A-T

http://identifiers.org/hco/17/GRCh38#9825619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67662205-C-A

9825619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67662205-C-T

9825633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67662192-G-A

9825633-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67662192-G-T

9825682-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67662153-T-G

http://identifiers.org/hco/17/GRCh38#9825701-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67662145-C-A

9825701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67662145-C-T

9825740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67662114-T-C

9825808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67662051-G-A

9825808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67662051-G-T

9825827-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67662031-G-C

9825827-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67662031-G-T

http://identifiers.org/hco/17/GRCh38#9825918-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67661955-C-A

9825918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 67661955-C-T

9826078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 67661799-G-A

9826078-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 67661799-G-C

http://identifiers.org/hco/17/GRCh38#9826115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67661762-C-A

9826130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 67661753-G-A

9826130-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant, stop_gained
orthologous variants: 67661753-G-T

9826150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 67661733-T-C

9826151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 67661732-G-T

9826203-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 67661680-C-G

http://identifiers.org/hco/17/GRCh38#9828215-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67660453-A-C

9828216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67660452-T-C

9828447-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67660245-T-A

9828447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67660245-T-C

9828653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 67660022-A-G

9828664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 67660012-C-T

9828776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67659899-G-A

9829447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67659263-A-G

9829739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67658962-C-T

9830040-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67658463-T-A

9830076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67658427-A-G

9830233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67657890-G-A

9830291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67657835-C-T

9830395-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67657736-G-C

9830452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67657681-A-G

9830684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67657444-A-G

9830848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67657076-T-C

http://identifiers.org/hco/17/GRCh38#9830998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67656927-C-A

9830998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67656927-C-T

9833077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67655786-A-G

9833797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67655682-G-T

9833860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 67655616-G-A

9833860-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 67655616-G-T

9833909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67655567-T-C

http://identifiers.org/hco/17/GRCh38#9833916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67655560-C-A

9833936-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67655540-G-T

9833948-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67655528-A-T

http://identifiers.org/hco/17/GRCh38#9833950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67655526-C-A

9833950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67655526-C-T

9833972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67655505-A-G

9834158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67655226-C-T

9834436-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67654974-C-G

9834436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67654974-C-T

http://identifiers.org/hco/17/GRCh38#9834437-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67654973-A-C

9834444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67654966-A-G

9834444-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67654966-A-T

9834549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 67654837-G-A

9834549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 67654837-G-T

9834598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 67654773-A-G

9834645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 67654701-T-C

9834683-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 67654664-G-C

9834792-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67654569-T-A

9834829-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67654532-C-G

9834829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67654532-C-T

9834836-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67654524-G-T

http://identifiers.org/hco/17/GRCh38#9834840-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67654520-A-C

9834840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67654520-A-G

9834841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67654519-C-T

http://identifiers.org/hco/17/GRCh38#9834884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67654474-C-A

9834884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67654474-C-T

9834903-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67654455-G-T

9835324-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67654286-G-C

9835568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67654068-G-A

9835719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67653936-C-T

9836090-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 67653896-T-A

9836090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 67653896-T-C

9836206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 67653792-C-T

9836257-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 67653741-G-C

9836257-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 67653741-G-T

9836284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 67653714-G-A

9836284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 67653714-G-T

9836302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67653694-C-T

http://identifiers.org/hco/17/GRCh38#9836397-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#67653598-C-A

9836397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, stop_gained, synonymous_variant, undefined
orthologous variants: 67653598-C-T

9838208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67652732-G-A

9838208-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67652732-G-T

9838363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 67652657-C-T

9838429-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 67652608-C-G

9838621-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67652429-T-G

9838711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67652339-C-T

http://identifiers.org/hco/17/GRCh38#9838738-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67652308-A-C

9838740-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67652306-C-G

9839096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67652057-A-G

http://identifiers.org/hco/17/GRCh38#9839147-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67652007-A-C

9839259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67651893-T-C

9839259-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67651893-T-G

http://identifiers.org/hco/17/GRCh38#9839432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67651744-C-A

9839434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67651742-A-G

9839489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67651691-A-G

9839706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67651474-C-T

9839750-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67651434-T-A

9839799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67651379-A-G

9840570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67649790-C-T

9840909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67649488-A-G

9842090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 67648849-G-A

9842142-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 67648794-G-T

9842145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 67648783-T-C

9842272-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67648675-C-G

http://identifiers.org/hco/17/GRCh38#9842379-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67648571-C-A

9842379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67648571-C-T

http://identifiers.org/hco/17/GRCh38#9842677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#67648264-C-A

9842683-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 67648258-T-A

http://identifiers.org/hco/17/GRCh38#9842696-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#67648245-C-A

9842696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 67648245-C-T

http://identifiers.org/hco/17/GRCh38#9842733-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67648210-C-A

9842733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67648210-C-T

http://identifiers.org/hco/17/GRCh38#9842763-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#67648172-C-A

9842763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 67648172-C-T

9843044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67647962-G-A

9843044-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67647962-G-C

9843055-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67647951-G-T

9843322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67647795-C-T

9843773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67646517-T-C

9843959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67646388-C-T

9844003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67646348-A-G

9844145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67646193-G-A

9844147-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67646191-G-C

9844222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67646051-G-A

9844274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67646001-G-A

http://identifiers.org/hco/17/GRCh38#9844323-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67645951-A-C

9844384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67645927-G-T

http://identifiers.org/hco/17/GRCh38#9844446-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67645867-C-A

9844446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67645867-C-T

9847999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67645267-C-T

9848003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67645263-A-G

9848100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67645176-T-C

9848460-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67644838-T-A

9848637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67644543-T-C

9848826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67644360-T-C

9848953-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67644250-T-A

9848985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67644208-G-A

http://identifiers.org/hco/17/GRCh38#9850069-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67641479-C-A

9850076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67641472-A-G

9850115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67641433-G-A

http://identifiers.org/hco/17/GRCh38#9850173-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67641386-A-C

9850510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67641139-G-A

9850692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67640978-C-T

9851187-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67640795-A-T

9851201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67640782-C-T

9851598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67639690-T-C

http://identifiers.org/hco/17/GRCh38#9851637-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67639652-A-C

9854204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67637931-A-G

9854246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67637890-C-T

9854356-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67637786-A-T

http://identifiers.org/hco/17/GRCh38#9854419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67637720-C-A

9854419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67637720-C-T

9854436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67637703-G-T

9854564-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 67637568-T-G

http://identifiers.org/hco/17/GRCh38#9854577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67637555-C-A

9854577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 67637555-C-T

9854607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67637525-T-C

9855203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67637443-C-T

http://identifiers.org/hco/17/GRCh38#9855802-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67636980-A-C

9855866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67636936-C-T

http://identifiers.org/hco/17/GRCh38#9856184-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67636642-C-A

9856184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67636642-C-T

9856461-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67636415-G-C

9856540-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67636341-T-A

9856578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67636312-A-G

9856621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67636261-G-A

9856621-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67636261-G-T

9857282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67635957-A-G

9857282-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67635957-A-T

9857367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67635897-T-C

9857382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67635878-T-C

9857385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67635875-T-C

9857653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67635643-G-A

9857653-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67635643-G-C

9857691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67635616-A-G

9857715-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67635596-T-A

9857753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67635560-C-T

9857772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67635540-A-G

9857852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67635487-A-G

9857853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67635486-C-T

http://identifiers.org/hco/17/GRCh38#9859885-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67633228-C-A

9859885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67633228-C-T

9859960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 67633160-T-C

9859991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 67633129-G-A

9860076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, stop_gained
orthologous variants: 67633044-G-A

http://identifiers.org/hco/17/GRCh38#9860219-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67632911-C-A

9860219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67632911-C-T

9860231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67632899-G-A

9860231-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67632899-G-T

9860253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67632866-G-A

9860253-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67632866-G-T

9860313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67632796-A-G

9860449-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67632665-C-G

9860522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67632590-T-C

9860607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67632502-C-T

9860759-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67632306-T-G

http://identifiers.org/hco/17/GRCh38#9860777-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67632289-A-C

9860780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67632286-A-G

9860906-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67632161-G-T

9861025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67632036-T-C

9861025-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67632036-T-G

9861037-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67632019-T-G

http://identifiers.org/hco/17/GRCh38#9861063-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67631984-C-A

9861063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67631984-C-T

9861076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67631970-G-A

9861079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67631967-G-A

9861079-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67631967-G-C

9861087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67631960-G-A

9861095-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67631952-G-T

9861166-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 67631885-G-C

9861166-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 67631885-G-T

http://identifiers.org/hco/17/GRCh38#9861173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67631878-C-A

9861173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 67631878-C-T

9861258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67631793-A-G

9861266-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67631785-A-T

http://identifiers.org/hco/17/GRCh38#9861267-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67631784-A-C

9861290-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67631761-A-G

9861320-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67631731-G-T

9861342-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67631708-T-A

9861342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67631708-T-C

http://identifiers.org/hco/17/GRCh38#9861352-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67631698-A-C

9861352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67631698-A-G

http://identifiers.org/hco/17/GRCh38#9861354-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67631692-A-C

9861355-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67631691-G-C

9861427-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67631629-G-T

9861461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67631596-G-A

9861904-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67631111-T-A

9861904-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67631111-T-G

9861987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67631028-G-A

9862073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 67630949-A-G

http://identifiers.org/hco/17/GRCh38#9862111-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67630908-C-A

http://identifiers.org/hco/17/GRCh38#9862121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67630897-C-A

9862121-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67630897-C-G

9862121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67630897-C-T

9862139-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67630877-G-C

http://identifiers.org/hco/17/GRCh38#9862155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67630860-C-A

9862155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67630860-C-T

9862163-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67630852-T-A

9862163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67630852-T-C

9862163-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67630852-T-G

http://identifiers.org/hco/17/GRCh38#9862165-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67630850-C-A

9862185-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67630830-T-A

9862185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67630830-T-C

http://identifiers.org/hco/17/GRCh38#9862210-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67630805-A-C

9862210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67630805-A-G

9862223-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67630792-G-T

9862323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67630698-G-A

9862350-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67630671-A-T

9862370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67630643-G-T

9862714-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67629088-G-C

9862754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67629053-G-A

9862754-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67629053-G-C

http://identifiers.org/hco/17/GRCh38#9862832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67628995-C-A

9862832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67628995-C-T

9862896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67628938-C-T

9862917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67628921-A-G

9863078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67628775-C-T

9863212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67628639-C-T

9863671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67628215-T-C

9863782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67628124-C-T

9863836-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67628075-G-C

9864197-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67627724-C-G

http://identifiers.org/hco/17/GRCh38#9865088-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67627234-C-A

9865207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67627120-G-A

9865408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67626954-G-T

9865587-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 67626771-T-G

9865693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67626714-C-T

http://identifiers.org/hco/17/GRCh38#9865701-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67626706-A-C

http://identifiers.org/hco/17/GRCh38#9866915-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67626377-C-A

9867158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67625936-T-C

9867423-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67625699-T-A

9867614-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67625500-G-C

9867615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67625499-A-G

9867805-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67625296-C-G

9867805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67625296-C-T

9867877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67625223-G-A

9867886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67625214-C-T

9867899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67625201-C-T

9868319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67624237-T-C

9868328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67624227-A-G

9868555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67623987-A-G

9868640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67623904-G-A

9868777-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67623770-G-C

9868924-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67623638-C-G

9868924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67623638-C-T

9869026-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67623532-C-G

9869026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67623532-C-T

http://identifiers.org/hco/17/GRCh38#9869223-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67622900-C-A

http://identifiers.org/hco/17/GRCh38#9869552-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67622594-A-C

9869589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67622570-A-G

9869605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67622548-G-A

9869765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67622436-A-G

9869846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67622356-A-G

9870079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67622128-G-A

9870079-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67622128-G-C

9870100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67622107-G-A

http://identifiers.org/hco/17/GRCh38#9870421-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67621809-C-A

9870421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67621809-C-T

9870492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67621741-T-C

http://identifiers.org/hco/17/GRCh38#9870634-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67621654-C-A

9870634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67621654-C-T

9870658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67621633-G-A

9870658-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67621633-G-T

9870690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67621601-G-A

9870709-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67621583-T-A

9870709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67621583-T-C

http://identifiers.org/hco/17/GRCh38#9870710-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67621582-C-A

9870710-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67621582-C-G

9870710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67621582-C-T

9870842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 67621449-G-A

9870842-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 67621449-G-T

9870848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67621443-A-G

9870849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67621442-G-A

9870849-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67621442-G-T

http://identifiers.org/hco/17/GRCh38#9870866-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67621425-C-A

http://identifiers.org/hco/17/GRCh38#9870898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67621396-C-A

9870898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67621396-C-T

9870971-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67620941-A-T

9871399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67620336-T-C

9875027-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67618498-G-C

http://identifiers.org/hco/17/GRCh38#9875095-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67618430-A-C

9875665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67617953-G-A

9875741-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67617917-G-C

9875865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67617794-G-A

9877014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67616228-A-G

9877017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67616225-A-G

9877145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67616101-A-G

9877314-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67615934-G-T

9877319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67615929-G-A

http://identifiers.org/hco/17/GRCh38#9877358-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67615889-A-C

9877513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67615753-A-G

9877517-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67615745-C-G

9877517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67615745-C-T

9878220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67615118-C-T

9878390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67614952-T-C

9878391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67614951-C-T

9878418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67614924-G-A

9878418-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67614924-G-T

9878506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67614748-A-G

9878772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67614518-T-C

http://identifiers.org/hco/17/GRCh38#9879069-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67614220-C-A

9879071-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67614218-G-C

http://identifiers.org/hco/17/GRCh38#9879570-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67613621-A-C

9879592-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67613599-A-T

9879751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67613424-G-A

9879824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67613363-C-T

http://identifiers.org/hco/17/GRCh38#9879986-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67613243-A-C

9880075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67613172-G-A

9880253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67613034-G-A

9880253-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67613034-G-T

9880280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67613014-A-G

http://identifiers.org/hco/17/GRCh38#9880296-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67612988-C-A

9880296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67612988-C-T

9880321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67612975-A-G

http://identifiers.org/hco/17/GRCh38#9880329-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67612967-C-A

9880329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67612967-C-T

http://identifiers.org/hco/17/GRCh38#9880335-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67612961-C-A

9880335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67612961-C-T

http://identifiers.org/hco/17/GRCh38#9880336-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67612960-C-A

9880336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67612960-C-T

9880342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67612954-T-C

http://identifiers.org/hco/17/GRCh38#9880354-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67612942-C-A

9880354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67612942-C-T

9880357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67612939-T-C

http://identifiers.org/hco/17/GRCh38#9880391-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67612906-A-C

9880391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: missense variant
orthologous variants: 67612906-A-G

http://identifiers.org/hco/17/GRCh38#9880445-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67612852-A-C

9880749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67612560-G-A

9880859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67612449-A-G

9880884-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67612422-A-T

9881023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67612294-T-C

9881092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67612248-G-T

9881317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67612012-T-C

9881317-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67612012-T-G

9882069-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67610418-T-A

9882154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67610337-C-T

http://identifiers.org/hco/17/GRCh38#9882693-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67609926-A-C

9883197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67609214-G-A

9883556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67608866-A-G

9884622-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67607792-T-G

9884641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67607775-G-A

9884680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67607749-A-G

http://identifiers.org/hco/17/GRCh38#9885043-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67607395-A-C

http://identifiers.org/hco/17/GRCh38#9885464-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67607186-A-C

9885727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67606931-G-A

9885791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67606873-G-A

http://identifiers.org/hco/17/GRCh38#9885795-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67606869-C-A

9885795-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67606869-C-G

9885795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67606869-C-T

9886239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67606531-G-A

9886501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67606307-T-C

9886505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67606303-G-A

9886759-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67606078-T-C

9886873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67605736-C-T

9886932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67605670-A-G

9886984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67605619-C-T

9887137-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67603803-C-G

9887137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67603803-C-T

http://identifiers.org/hco/17/GRCh38#9887352-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#67603658-C-A

9887352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron_variant, undefined
orthologous variants: 67603658-C-T

http://identifiers.org/hco/17/GRCh38#9887811-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67603241-C-A

9887811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67603241-C-T

9888022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67603073-A-G

http://identifiers.org/hco/17/GRCh38#9888033-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67603057-C-A

9888033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67603057-C-T

9888097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67603011-G-A

9888097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67603011-G-T

9889288-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67600714-A-T

9889289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67600713-G-A

9889289-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67600713-G-C

9889289-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67600713-G-T

http://identifiers.org/hco/17/GRCh38#9889340-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67600663-C-A

9889340-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67600663-C-G

9889354-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67600649-T-G

http://identifiers.org/hco/17/GRCh38#9889358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67600645-C-A

9889358-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: intron variant
orthologous variants: 67600645-C-G

9889415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: missense variant
orthologous variants: 67600588-C-T

9889431-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: missense variant
orthologous variants: 67600572-G-C

9889431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: missense variant
orthologous variants: 67600572-G-T

9889439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: missense variant
orthologous variants: 67600564-G-A

9889442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: synonymous variant
orthologous variants: 67600561-C-T

9889502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: missense variant
orthologous variants: 67600501-G-A

9889502-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: missense variant
orthologous variants: 67600501-G-T

9889505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: missense variant
orthologous variants: 67600498-G-A

http://identifiers.org/hco/17/GRCh38#9889531-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67600472-A-C

9889532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: missense variant
orthologous variants: 67600471-C-T

9889533-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: missense variant
orthologous variants: 67600470-T-A

http://identifiers.org/hco/17/GRCh38#9889618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67600394-C-A

9889705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: stop retained variant
orthologous variants: 67600307-G-A

9889730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3 prime UTR variant
orthologous variants: 67600283-T-C

9889861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3 prime UTR variant
orthologous variants: 67600181-T-C

9889862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3 prime UTR variant
orthologous variants: 67600180-C-T

9889872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3 prime UTR variant
orthologous variants: 67600170-G-A

http://identifiers.org/hco/17/GRCh38#9889876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67600166-C-A

9889878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3 prime UTR variant
orthologous variants: 67600164-G-A

http://identifiers.org/hco/17/GRCh38#9889895-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67600149-C-A

http://identifiers.org/hco/17/GRCh38#9889910-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67600135-C-A

9889910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3 prime UTR variant
orthologous variants: 67600135-C-T

9889932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3 prime UTR variant
orthologous variants: 67600105-G-A

http://identifiers.org/hco/17/GRCh38#9889949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67600088-C-A

9889959-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3 prime UTR variant
orthologous variants: 67600078-C-G

http://identifiers.org/hco/17/GRCh38#9890014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67600024-C-A

9890014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3 prime UTR variant
orthologous variants: 67600024-C-T

9890037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3 prime UTR variant
orthologous variants: 67600001-T-C

9890037-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3 prime UTR variant
orthologous variants: 67600001-T-G

9890051-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3 prime UTR variant
orthologous variants: 67599991-T-G

9890085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3 prime UTR variant
orthologous variants: 67599957-G-T

http://identifiers.org/hco/17/GRCh38#9890121-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67599922-A-C

http://identifiers.org/hco/17/GRCh38#9890122-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67599921-A-C

9890142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3 prime UTR variant
orthologous variants: 67599899-T-C

9890143-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3 prime UTR variant
orthologous variants: 67599898-G-T

9890144-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3 prime UTR variant
orthologous variants: 67599897-G-T

http://identifiers.org/hco/17/GRCh38#9890207-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67599834-C-A

9890320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3 prime UTR variant
orthologous variants: 67599770-C-T

http://identifiers.org/hco/17/GRCh38#9890326-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67599764-C-A

9890326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3 prime UTR variant
orthologous variants: 67599764-C-T

9890397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3 prime UTR variant
orthologous variants: 67599687-T-C

9890525-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3 prime UTR variant
orthologous variants: 67598450-T-A

9890525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3 prime UTR variant
orthologous variants: 67598450-T-C

http://identifiers.org/hco/17/GRCh38#9890558-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67598417-A-C

9890558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3 prime UTR variant
orthologous variants: 67598417-A-G

9890590-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3 prime UTR variant
orthologous variants: 67598386-T-G

http://identifiers.org/hco/17/GRCh38#9890717-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67598278-A-C

9890717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3 prime UTR variant
orthologous variants: 67598278-A-G

http://identifiers.org/hco/17/GRCh38#9890722-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67598273-A-C

http://identifiers.org/hco/17/GRCh38#9890827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67598195-C-A

9890827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3 prime UTR variant
orthologous variants: 67598195-C-T

9890846-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3 prime UTR variant
orthologous variants: 67598176-G-T

http://identifiers.org/hco/17/GRCh38#9890898-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67598105-A-C

9890898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3 prime UTR variant
orthologous variants: 67598105-A-G

9890902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3 prime UTR variant
orthologous variants: 67598101-A-G

9890912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3 prime UTR variant
orthologous variants: 67598091-A-G

http://identifiers.org/hco/17/GRCh38#9890915-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67598088-C-A

9890915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3 prime UTR variant
orthologous variants: 67598088-C-T

9890942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3 prime UTR variant
orthologous variants: 67598061-G-A

9890942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3 prime UTR variant
orthologous variants: 67598061-G-T

9890953-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3 prime UTR variant
orthologous variants: 67598050-G-T

http://identifiers.org/hco/17/GRCh38#9891006-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67597997-C-A

9891041-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3 prime UTR variant
orthologous variants: 67597889-G-T

9891057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3 prime UTR variant
orthologous variants: 67597863-G-A

9891057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3 prime UTR variant
orthologous variants: 67597863-G-T

9891058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3 prime UTR variant
orthologous variants: 67597862-G-A

9891058-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3 prime UTR variant
orthologous variants: 67597862-G-T

9891074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3 prime UTR variant
orthologous variants: 67597826-G-A

9891094-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3 prime UTR variant
orthologous variants: 67597784-G-T

9891099-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3 prime UTR variant
orthologous variants: 67597779-T-A

9891103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3 prime UTR variant
orthologous variants: 67597775-C-T

http://identifiers.org/hco/17/GRCh38#9891315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67597512-C-A

http://identifiers.org/hco/17/GRCh38#9891327-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67597500-C-A

http://identifiers.org/hco/17/GRCh38#9891396-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67597449-C-A

http://identifiers.org/hco/17/GRCh38#9891475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67597373-C-A

9891475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3 prime UTR variant
orthologous variants: 67597373-C-T

9891665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3 prime UTR variant
orthologous variants: 67597204-A-G

9891694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3 prime UTR variant
orthologous variants: 67597175-G-A

9891720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3 prime UTR variant
orthologous variants: 67597150-G-A

9891720-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3 prime UTR variant
orthologous variants: 67597150-G-T

9891721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3 prime UTR variant
orthologous variants: 67597149-T-C

9891748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3 prime UTR variant
orthologous variants: 67597125-G-A

http://identifiers.org/hco/17/GRCh38#9891764-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67597109-C-A

9891764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3 prime UTR variant
orthologous variants: 67597109-C-T

http://identifiers.org/hco/17/GRCh38#9891797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67597076-C-A

9891797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3 prime UTR variant
orthologous variants: 67597076-C-T

9891817-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3 prime UTR variant
orthologous variants: 67597058-T-A

9891817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3 prime UTR variant
orthologous variants: 67597058-T-C

9891922-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3 prime UTR variant
orthologous variants: 67596957-G-T

9891957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3 prime UTR variant
orthologous variants: 67596919-T-C

http://identifiers.org/hco/17/GRCh38#9891961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67596915-C-A

9891961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3 prime UTR variant
orthologous variants: 67596915-C-T

http://identifiers.org/hco/17/GRCh38#9892034-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4325
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67596842-C-A