15682189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron variant
orthologous variants: 141394268-C-T

15682193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron variant
orthologous variants: 141394264-C-T

15682324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron variant
orthologous variants: 141394153-G-A

15682342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron variant
orthologous variants: 141394136-T-C

http://identifiers.org/hco/1/GRCh38#15682618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141393850-C-A

http://identifiers.org/hco/1/GRCh38#15682628-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141393840-C-A

15683652-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron variant
orthologous variants: 141392181-T-A

15683781-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron variant
orthologous variants: 141392046-T-G

15684192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron variant
orthologous variants: 141391565-C-T

http://identifiers.org/hco/1/GRCh38#15684371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141391396-C-A

15684371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 141391396-C-T

http://identifiers.org/hco/1/GRCh38#15684373-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141391394-C-A

15684373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 141391394-C-T

15684483-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 141391275-C-G

15684483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 141391275-C-T

15684559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 141391229-A-G

15684559-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 141391229-A-T

15684573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 141391215-G-A

15684573-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 141391215-G-C

15684573-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 141391215-G-T

http://identifiers.org/hco/1/GRCh38#15684689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141391103-C-A

15684689-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141391103-C-G

15684689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141391103-C-T

http://identifiers.org/hco/1/GRCh38#15684695-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141391097-C-A

15684695-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141391097-C-G

15684695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141391097-C-T

http://identifiers.org/hco/1/GRCh38#15684738-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141391079-A-C

15684738-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141391079-A-T

15684765-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 141391052-G-T

15684859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141390959-G-A

15685159-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141390713-G-C

15685272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141390607-A-G

http://identifiers.org/hco/1/GRCh38#15689371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141388586-C-A

15689371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141388586-C-T

15689594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141388405-T-C

15689595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141388404-G-A

15689766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141388200-T-C

15690079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141387895-G-A

15690079-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141387895-G-T

15690207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141387770-G-A

15690213-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141387764-A-T

15690408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141387603-T-C

15690415-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141387596-G-C

http://identifiers.org/hco/1/GRCh38#15690692-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141387316-A-C

15692324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141386757-A-G

15693542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141386390-G-A

15693878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141386093-G-T

15694513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141385804-T-C

15694558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141385749-A-G

http://identifiers.org/hco/1/GRCh38#15695167-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141385198-C-A

15695249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141385119-G-A

15695257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141385111-A-G

15695268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141385101-A-G

15695298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141385073-A-G

15695314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141385059-C-T

15697131-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141383598-G-C

15697294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141383467-C-T

15697482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141383305-C-T

15697496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141383291-T-C

15700677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141381358-A-G

15700840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141381201-G-A

15701042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141381046-G-A

15701042-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141381046-G-T

15701043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141381045-G-A

http://identifiers.org/hco/1/GRCh38#15701103-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141381002-A-C

15701103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141381002-A-G

15701292-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141380786-G-C

15701697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141380243-A-G

15702248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141379669-G-A

15702249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141379668-C-T

15702268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141379649-C-T

15702328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141379593-C-T

15703283-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141379275-G-T

15703401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141379105-C-T

15703493-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141379041-C-G

15703493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141379041-C-T

15703837-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141378721-G-C

15703861-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141378697-G-C

15704139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141378050-C-T

http://identifiers.org/hco/1/GRCh38#15704180-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141378031-C-A

15704180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141378031-C-T

15704311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141377917-T-C

15704319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141377909-T-C

http://identifiers.org/hco/1/GRCh38#15714604-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141371066-A-C

15714696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141370994-G-A

15714902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141370819-C-T

http://identifiers.org/hco/1/GRCh38#15714986-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141370735-C-A

15715122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141370613-A-G

http://identifiers.org/hco/1/GRCh38#15716288-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141370014-C-A

15716288-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 141370014-C-G

15716288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 141370014-C-T

15716327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 141369975-C-T

http://identifiers.org/hco/1/GRCh38#15716382-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141369941-C-A

15716382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141369941-C-T

http://identifiers.org/hco/1/GRCh38#15716471-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141369902-C-A

15716476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141369897-G-A

15716476-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141369897-G-C

15716585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141369873-T-C

15716698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141369833-T-C

http://identifiers.org/hco/1/GRCh38#15716792-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141369739-C-A

15716792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 141369739-C-T

http://identifiers.org/hco/1/GRCh38#15716850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141369705-C-A

15716850-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141369705-C-G

15716850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141369705-C-T

15716899-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141369675-T-A

15716899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141369675-T-C

15716933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141369637-G-A

15717477-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141369580-T-G

15717635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141369466-G-A

15717650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141369451-G-A

http://identifiers.org/hco/1/GRCh38#15718084-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141369214-C-A

15718084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141369214-C-T

15718134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141369162-G-T

15718393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141368957-G-A

15718393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141368957-G-T

15718453-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141368899-T-A

15718477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141368875-A-G

http://identifiers.org/hco/1/GRCh38#15718486-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141368866-C-A

15718486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141368866-C-T

15718488-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141368864-G-T

15718505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141368847-A-G

http://identifiers.org/hco/1/GRCh38#15718512-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141368839-C-A

15718512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141368839-C-T

15718629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141368722-A-G

15718867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141368516-T-C

15718901-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141368482-C-G

15719739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 141367166-C-T

http://identifiers.org/hco/1/GRCh38#15719794-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141367111-C-A

15719924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron variant
orthologous variants: 141366981-A-G

15719938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron variant
orthologous variants: 141366966-A-G

15719942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron variant
orthologous variants: 141366962-A-G

http://identifiers.org/hco/1/GRCh38#15719968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141366934-C-A

15719968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron variant
orthologous variants: 141366934-C-T

http://identifiers.org/hco/1/GRCh38#15719984-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141366918-C-A

15719984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron variant
orthologous variants: 141366918-C-T

http://identifiers.org/hco/1/GRCh38#15720044-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141366477-C-A

http://identifiers.org/hco/1/GRCh38#15720054-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141366467-C-A

http://identifiers.org/hco/1/GRCh38#15720203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141366366-C-A

15720203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron variant
orthologous variants: 141366366-C-T

15720228-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron variant
orthologous variants: 141366350-A-G

15720278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron variant
orthologous variants: 141366296-G-A

15720278-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron variant
orthologous variants: 141366296-G-C

15720278-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron variant
orthologous variants: 141366296-G-T

http://identifiers.org/hco/1/GRCh38#15720349-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141366233-C-A

15720434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 141366169-A-G

15720434-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 141366169-A-T

15720526-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 141365844-G-T

15720530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 141365840-G-A

15720530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 141365840-G-T

15720655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141365740-G-A

15720655-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141365740-G-T

15720662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141365733-G-A

15720662-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141365733-G-T

15720688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141365719-A-G

15720754-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141365658-T-G

15720781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141365241-A-G

15720781-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141365241-A-T

15720886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 141365129-G-A

15720886-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 141365129-G-C

15720886-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 141365129-G-T

15720932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 141365091-T-C

15720932-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 141365091-T-G

15720941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 141365077-A-G

15720941-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 141365077-A-T

15720973-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 141365047-A-T

http://identifiers.org/hco/1/GRCh38#15721011-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141365010-A-C

15721011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141365010-A-G

15721100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141364942-C-T

http://identifiers.org/hco/1/GRCh38#15721196-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141364906-A-C

15721196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141364906-A-G

http://identifiers.org/hco/1/GRCh38#15721262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141364858-C-A

15721262-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141364858-C-G

15721262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141364858-C-T

http://identifiers.org/hco/1/GRCh38#15721267-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141364853-C-A

15721280-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141364840-T-A

15721280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141364840-T-C

15721280-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141364840-T-G

http://identifiers.org/hco/1/GRCh38#15721289-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141364831-C-A

http://identifiers.org/hco/1/GRCh38#15721491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141364631-C-A

http://identifiers.org/hco/1/GRCh38#15721505-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141364617-A-C

15721505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141364617-A-G

15721629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141364512-A-G

15721678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141364467-C-T

15721685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141364460-A-G

15721700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141364444-G-A

15722503-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141363793-G-C

15722669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141363713-G-T

http://identifiers.org/hco/1/GRCh38#15722809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141363580-C-A

15722809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141363580-C-T

15722940-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141363438-G-C

15722942-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141363436-C-G

15723017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141363342-C-T

15723051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141363316-C-T

15723096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141363269-C-T

15723210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 141363145-G-A

15723364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141363003-T-C

15723364-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141363003-T-G

http://identifiers.org/hco/1/GRCh38#15723840-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141362821-C-A

15724008-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141362657-T-G

15724067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141362595-C-T

15724103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141362562-G-A

15724572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141362461-G-A

15724701-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141362334-T-C

15724938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141362128-G-A

15724938-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141362128-G-T

15725175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141361920-T-C

http://identifiers.org/hco/1/GRCh38#15725406-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141361698-C-A

15725406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 141361698-C-T

15725448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 141361656-T-C

15725556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141361551-A-G

15725556-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141361551-A-T

15725575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141361531-G-A

15725575-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141361531-G-C

15726939-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141359955-A-T

http://identifiers.org/hco/1/GRCh38#15726996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141359903-C-A

15726996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141359903-C-T

http://identifiers.org/hco/1/GRCh38#15727075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141359824-C-A

15727075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 141359824-C-T

15727126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 141359773-G-T

15727147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 141359752-A-G

15727237-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 141359662-T-G

15727427-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 141359463-G-T

http://identifiers.org/hco/1/GRCh38#15727619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141359265-C-A

15727619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 141359265-C-T

15727642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 141359224-G-A

15727642-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 141359224-G-T

15727662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 141359204-G-A

15727681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 141359185-G-A

15727681-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 141359185-G-T

http://identifiers.org/hco/1/GRCh38#15727733-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141359121-A-C

15727733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 141359121-A-G

15727733-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 141359121-A-T

http://identifiers.org/hco/1/GRCh38#15727886-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141358987-C-A

15727987-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141358960-G-C

15727987-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141358960-G-T

15728188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141358783-G-A

15728540-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141358478-T-A

15728558-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141358458-T-A

15728558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141358458-T-C

15728653-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141358381-G-T

15728660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141358374-C-T

15728846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141358211-G-A

15728846-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141358211-G-T

15728960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141358105-G-A

15728960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141358105-G-T

http://identifiers.org/hco/1/GRCh38#15728995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141358059-C-A

15728995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141358059-C-T

15728996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141358058-G-A

15728996-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141358058-G-C

15728996-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141358058-G-T

http://identifiers.org/hco/1/GRCh38#15729175-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141357896-A-C

http://identifiers.org/hco/1/GRCh38#15729205-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141357866-C-A

15729205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141357866-C-T

15729219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141357852-G-A

http://identifiers.org/hco/1/GRCh38#15729333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141357760-C-A

15729333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141357760-C-T

15729436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141357651-T-C

15729436-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141357651-T-G

http://identifiers.org/hco/1/GRCh38#15729708-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141357417-C-A

15729708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141357417-C-T

15730004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141357162-G-A

15730004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141357162-G-T

http://identifiers.org/hco/1/GRCh38#15730012-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141357154-C-A

15730012-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141357154-C-G

15730012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141357154-C-T

15730013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141357153-G-A

15730013-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141357153-G-T

http://identifiers.org/hco/1/GRCh38#15730017-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141357148-A-C

15730017-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141357148-A-T

http://identifiers.org/hco/1/GRCh38#15730021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141357144-C-A

15730021-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141357144-C-G

http://identifiers.org/hco/1/GRCh38#15730489-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141356988-C-A

15730489-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141356988-C-G

15730489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141356988-C-T

15730491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141356986-G-A

15730491-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141356986-G-T

15730495-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141356982-T-A

15730495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141356982-T-C

http://identifiers.org/hco/1/GRCh38#15730511-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141356968-C-A

15730511-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141356968-C-G

15730511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141356968-C-T

15730574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141356907-G-A

15730574-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 141356907-G-T

http://identifiers.org/hco/1/GRCh38#15730625-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141356856-C-A

15730625-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141356856-C-G

15730625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141356856-C-T

15730667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141356814-G-T

http://identifiers.org/hco/1/GRCh38#15730736-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141356745-C-A

15730736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141356745-C-T

http://identifiers.org/hco/1/GRCh38#15730826-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141356699-C-A

15730826-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141356699-C-G

http://identifiers.org/hco/1/GRCh38#15730854-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141356671-C-A

http://identifiers.org/hco/1/GRCh38#15731044-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141356563-C-A

http://identifiers.org/hco/1/GRCh38#15731081-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141356526-C-A

15731081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141356526-C-T

http://identifiers.org/hco/1/GRCh38#15731250-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141356397-A-C

15731250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141356397-A-G

15731285-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141356365-T-A

http://identifiers.org/hco/1/GRCh38#15731343-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141356299-C-A

15731343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141356299-C-T

15731498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141356191-C-T

15731640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141356088-T-C

15731742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141355994-A-G

http://identifiers.org/hco/1/GRCh38#15731797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141355930-C-A

http://identifiers.org/hco/1/GRCh38#15731811-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141355870-C-A

15731811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141355870-C-T

http://identifiers.org/hco/1/GRCh38#15731812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141355869-C-A

15731812-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141355869-C-G

15731812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141355869-C-T

15732068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141355571-A-G

http://identifiers.org/hco/1/GRCh38#15732100-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141355554-C-A

15732100-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141355554-C-G

15732100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141355554-C-T

http://identifiers.org/hco/1/GRCh38#15732246-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141355522-C-A

15732246-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141355522-C-G

15732246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141355522-C-T

15732260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141355508-A-G

15732632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 141355156-G-A

http://identifiers.org/hco/1/GRCh38#15733510-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141354199-A-C

15733651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141354120-A-G

15733651-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141354120-A-T

15733851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141353962-G-A

15733902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141353911-C-T

15733908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 141353905-C-T

15733915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141353898-C-T

15733946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141353867-T-C

http://identifiers.org/hco/1/GRCh38#15734299-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141353528-C-A

15734299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 141353528-C-T

15734300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 141353527-G-A

15734300-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 141353527-G-C

15734300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 141353527-G-T

http://identifiers.org/hco/1/GRCh38#15734303-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141353524-A-C

15734303-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 141353524-A-T

15734380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 141353422-C-T

15734396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 141353406-G-A

http://identifiers.org/hco/1/GRCh38#15734432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141353372-C-A

15734432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 141353372-C-T

http://identifiers.org/hco/1/GRCh38#15734492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141353331-C-A

15734492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 141353331-C-T

http://identifiers.org/hco/1/GRCh38#15734496-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141353327-C-A

http://identifiers.org/hco/1/GRCh38#15734528-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141353295-C-A

15734528-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 141353295-C-G

15734528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 141353295-C-T

15734621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 141353186-G-A

15734621-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 141353186-G-T

15734644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 141353163-T-C

15734651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29131
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 141353156-G-A