http://identifiers.org/hco/12/GRCh38#50505022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#99936567-C-A

50505022-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 99936567-C-G

50505022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 99936567-C-T

http://identifiers.org/hco/12/GRCh38#50505081-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#99936633-C-A

50505081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 99936633-C-T

50505133-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 99936683-G-T

50505169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 99936719-C-T

50505526-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99936956-G-C

50505696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99937060-G-A

50505696-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99937060-G-T

50506050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99937401-G-A

50506050-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99937401-G-T

50506343-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99937691-T-G

50506837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99938142-T-C

50506854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99938166-A-G

50506897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99938217-G-A

50506925-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99938245-T-G

50507181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99938486-A-G

50507909-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99938894-T-A

50507909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99938894-T-C

50508181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99939137-G-A

50508226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99939183-A-G

http://identifiers.org/hco/12/GRCh38#50508258-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99939209-A-C

50508632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99939512-C-T

50508706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99939580-T-C

http://identifiers.org/hco/12/GRCh38#50508710-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99939584-A-C

50508710-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99939584-A-T

50509151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99939734-C-T

50509229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99939815-A-G

50509243-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99939829-C-G

50509359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99939923-A-G

50509471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99940040-A-G

50509556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99940117-A-G

50509697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99940226-G-A

50509788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99940293-C-T

http://identifiers.org/hco/12/GRCh38#50512478-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99943034-C-A

50512478-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99943034-C-G

50512516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99943077-T-C

50513204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99943429-A-G

http://identifiers.org/hco/12/GRCh38#50515187-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99944196-A-C

50515229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99944235-C-T

50515235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99944241-G-A

50517640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99945778-C-T

50518095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99946153-C-T

50529888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99946638-G-A

50531780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99948480-G-A

50531780-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99948480-G-T

50531871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99948548-C-T

50531971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99948604-G-A

50532049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99948667-G-T

50537753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99950594-A-G

50537795-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99950626-G-T

http://identifiers.org/hco/12/GRCh38#50541440-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99957828-C-A

50541440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99957828-C-T

50542378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99958441-A-G

50542407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99958469-A-G

50542407-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99958469-A-T

50542554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99958590-G-A

50542862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99958880-C-T

50548117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99964044-A-G

50548185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99964105-T-C

50548257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99964171-G-A

50549037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99964626-T-C

http://identifiers.org/hco/12/GRCh38#50549103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#99964692-C-A

50549103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99964692-C-T

50550479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99966420-C-T

50550696-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99966930-G-T

50555831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99971911-T-C

50555844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99971924-A-G

50555853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99971933-G-A

50555877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99971957-C-T

50556546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99972293-T-C

50557035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99972425-C-T

50557091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99972474-C-T

50557127-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99972507-T-G

50559268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99973792-G-A

50559268-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99973792-G-T

50568518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99974888-G-A

50568663-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99975030-T-G

50568735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99975102-T-C

http://identifiers.org/hco/12/GRCh38#50569494-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99975921-A-C

50569932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99977075-A-G

50570083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99977194-G-A

50570241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99977319-T-C

50571815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99978326-C-T

50571847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99978350-C-T

50572526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99979259-G-A

50572526-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99979259-G-C

50572977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99979693-G-A

http://identifiers.org/hco/12/GRCh38#50573010-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99979727-C-A

50573118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99979817-C-T

http://identifiers.org/hco/12/GRCh38#50573122-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99979821-C-A

50573122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99979821-C-T

50573263-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99979936-T-G

50573385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99980012-C-T

50573520-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99980117-G-C

50573521-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99980118-A-T

50573594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99980175-G-A

50573651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99980232-C-T

50573747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99980298-A-G

50573753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99980304-A-G

50574471-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99980990-G-T

50574489-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99981005-T-G

50574701-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99981203-G-C

50574910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99981405-C-T

http://identifiers.org/hco/12/GRCh38#50580248-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99986194-C-A

50581504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99987684-A-G

http://identifiers.org/hco/12/GRCh38#50581742-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99987891-C-A

50582095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99988146-A-G

50582126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99988173-C-T

50582600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99988295-C-T

50582710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99988399-C-T

50597253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99994703-C-T

50597527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99994973-A-G

50597555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99994983-G-A

50597662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99995123-C-T

50600864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99997046-G-A

50601748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99998109-C-T

50602001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99998344-C-T

http://identifiers.org/hco/12/GRCh38#50602060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99998403-C-A

50602121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99998457-T-C

50604047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99999399-C-T

50606399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-G

50606642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

50606738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

50610176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-G

50610176-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-T

50610236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-C

50610272-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-T

50610418-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-C

50614171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100005919-C-T

50614191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100005936-G-A

50614477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100006186-A-G

50614525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100006229-C-T

http://identifiers.org/hco/12/GRCh38#50614542-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#100006246-A-C

50614542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100006246-A-G

50614599-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100006280-G-C

50614603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100006284-C-T

50614619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100006300-C-T

50614627-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100006308-T-A

50614633-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100006314-G-T

50614706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100006367-C-T

50614817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100006461-C-T

50614847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100006483-C-T

50614849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100006485-G-A

50614881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100006517-T-C

50615013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100006628-C-T

50615500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100007343-A-G

50615693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100007689-G-A

50615767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100007755-A-G

50615997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100007988-A-G

50616222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100008220-C-T

50616317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100008298-C-T

http://identifiers.org/hco/12/GRCh38#50616418-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#100008384-A-C

50616483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100008499-C-T

50616566-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100008571-A-T

50616928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100009283-A-G

50616940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100009293-C-T

50616941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100009294-T-C

50621393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100011291-A-G

50622227-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100012101-G-C

http://identifiers.org/hco/12/GRCh38#50625086-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#100013011-A-C

50625161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100013107-A-G

50625601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100013418-G-A

50625754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100013516-T-C

http://identifiers.org/hco/12/GRCh38#50625835-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#100013591-C-A

50625835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100013591-C-T

50626080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100013811-G-A

50626080-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100013811-G-C

50626256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100013967-A-G

50626304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100014005-C-T

50633797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100018640-G-A

50633799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100018642-A-G

50633867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100018699-C-T

50633928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100018756-A-G

50634009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100018868-G-A

50634009-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100018868-G-T

50634528-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100019399-G-C

http://identifiers.org/hco/12/GRCh38#50634530-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#100019401-A-C

50634940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100020022-G-A

50634944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100020032-T-C

50635891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100022769-A-G

50636023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100022895-C-T

50636255-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100023086-T-G

50636941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100023681-A-G

50637336-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100024159-C-G

50637336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100024159-C-T

50637407-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100024223-T-G

50637717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100024536-G-A

50637970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100024759-A-G

50640680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100029739-T-C

50640701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100029760-A-G

50640726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 100029785-A-G

50640901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100029940-G-A

50640901-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100029940-G-C

50640901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100029940-G-T

http://identifiers.org/hco/12/GRCh38#50640916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#100029955-C-A

50640916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100029955-C-T

50642926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100030468-C-T

50643122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100030632-T-C

50644229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100032343-T-C

50644286-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100032400-T-C

50644489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100035131-G-A

50644508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100035150-T-C

50644578-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100035220-T-A

50644934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100035541-G-A

50644955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100035573-A-G

http://identifiers.org/hco/12/GRCh38#50645073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#100035823-C-A

50645073-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100035823-C-G

50659840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100039608-C-T

50660112-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100039827-T-A

50660112-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100039827-T-G

http://identifiers.org/hco/12/GRCh38#50660123-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#100039838-A-C

50660123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100039838-A-G

50660123-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100039838-A-T

50660131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100039846-G-A

50660131-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100039846-G-C

50660131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100039846-G-T

http://identifiers.org/hco/12/GRCh38#50660359-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#100040065-C-A

50660359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100040065-C-T

http://identifiers.org/hco/12/GRCh38#50660409-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#100040104-A-C

50660409-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100040104-A-T

50660413-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100040108-T-A

50660413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100040108-T-C

50660415-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100040110-T-G

50660418-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100040113-T-C

50660418-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100040113-T-G

50660627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100040239-A-G

50660673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100040284-C-T

50660721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100040330-G-A

50660896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100040474-A-G

50660908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100040486-G-A

50660908-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100040486-G-T

50660912-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100040490-T-A

50662009-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100041708-C-G

50662028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100041727-A-G

50662221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100041910-T-C

50662237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100041926-C-T

50664104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100043153-A-G

50664180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100043223-G-A

50664357-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100043389-A-T

50664364-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100043396-T-G

50667503-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100046188-G-T

50668210-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100047062-C-G

http://identifiers.org/hco/12/GRCh38#50668952-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#100047684-C-A

50668952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100047684-C-T

http://identifiers.org/hco/12/GRCh38#50671079-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#100048929-C-A

50671079-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100048929-C-G

50671079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100048929-C-T

50671116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100048965-A-G

50671116-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100048965-A-T

http://identifiers.org/hco/12/GRCh38#50671137-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#100048984-C-A

50671144-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100048991-C-G

50671407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100049253-T-C

50671447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100049293-C-T

50671448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100049294-C-T

50671469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100049315-A-G

http://identifiers.org/hco/12/GRCh38#50671489-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#100049334-C-A

50671489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100049334-C-T

http://identifiers.org/hco/12/GRCh38#50671498-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#100049340-C-A

50671498-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100049340-C-G

50671562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100049398-A-G

50671684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100049518-A-G

50672284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100050074-G-A

50672392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100050164-A-G

50672624-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100050353-C-G

50672625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100050354-A-G

50672736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100050461-C-T

50673183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100050865-T-C

50673185-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100050867-T-G

50673995-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100051395-G-C

50674081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100051447-G-A

50674281-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100051629-G-C

50674360-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100051940-G-T

50674366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100051946-G-A

50674366-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100051946-G-T

50674544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 100052102-A-G

50674736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100052292-T-C

50675130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100052595-T-C

50675186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100052659-G-A

50675297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100052880-G-A

50675297-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100052880-G-T

50675303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100052886-T-C

50675305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100052888-A-G

50675341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 100052927-G-A

50675357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 100052943-A-G

50675377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 100052963-A-G

50675414-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 100053000-A-T

50675432-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 100053018-T-G

50678728-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 100055100-C-G

50678788-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 100055160-C-G

50678788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 100055160-C-T

50680441-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron variant
orthologous variants: 100055559-G-C

50680522-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron variant
orthologous variants: 100055626-G-C

http://identifiers.org/hco/12/GRCh38#50680554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#100055655-C-A

50680563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron variant
orthologous variants: 100055661-G-A

50680563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron variant
orthologous variants: 100055661-G-T

50680599-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron variant
orthologous variants: 100055693-T-A

50680612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron variant
orthologous variants: 100055706-A-G

50680829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron variant
orthologous variants: 100055919-A-G

http://identifiers.org/hco/12/GRCh38#50680845-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#100055927-A-C

http://identifiers.org/hco/12/GRCh38#50682325-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#100057773-A-C

50682734-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron variant
orthologous variants: 100057850-T-G

50683033-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron variant
orthologous variants: 100058245-T-G

50683062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron variant
orthologous variants: 100058274-A-G

50683304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron variant
orthologous variants: 100058483-G-A

50683304-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron variant
orthologous variants: 100058483-G-T

50683366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron variant
orthologous variants: 100058563-T-C

50685214-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron variant
orthologous variants: 100059362-T-G

50685624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron variant
orthologous variants: 100059680-A-G

50685763-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron variant
orthologous variants: 100059778-A-T

http://identifiers.org/hco/12/GRCh38#50685790-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#100059804-C-A

50685790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: intron variant
orthologous variants: 100059804-C-T

50685985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100060011-T-C

50686098-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100060113-T-A

50686098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100060113-T-C

50686098-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100060113-T-G

http://identifiers.org/hco/12/GRCh38#50686197-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#100060196-C-A

http://identifiers.org/hco/12/GRCh38#50686225-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#100060222-A-C

50686341-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100060341-C-G

50686341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100060341-C-T

50686561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100060548-G-A

http://identifiers.org/hco/12/GRCh38#50686845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#100060794-C-A

50686928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100060871-A-G

50686936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100060879-T-C

50686936-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100060879-T-G

50686946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100060889-C-T

50686999-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100060960-G-T

50687031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100060995-G-A

50687031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100060995-G-T

50691034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100065722-G-A

50691252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100065939-G-A

50691252-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100065939-G-T

http://identifiers.org/hco/12/GRCh38#50692888-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#100067091-C-A

50692888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100067091-C-T

50692889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100067092-A-G

50692987-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 100067186-G-T

50693028-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100067226-T-A

http://identifiers.org/hco/12/GRCh38#50693040-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#100067238-A-C

50693041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100067239-G-A

50693041-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100067239-G-C

50693049-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100067247-T-G

http://identifiers.org/hco/12/GRCh38#50693066-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#100067261-C-A

50693112-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100067301-T-A

50693112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100067301-T-C

50693112-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100067301-T-G

http://identifiers.org/hco/12/GRCh38#50693117-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#100067306-C-A

50693117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100067306-C-T

50693132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100067321-A-G

50693137-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100067325-T-A

http://identifiers.org/hco/12/GRCh38#50694925-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#100068682-A-C

50694938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100068695-A-G

50694938-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100068695-A-T

50695107-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100068845-G-C

http://identifiers.org/hco/12/GRCh38#50695796-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#100069425-A-C

50695796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100069425-A-G

50695796-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100069425-A-T

50695814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100069446-G-A

50695814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100069446-G-T

50695915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 100069551-C-T

50695957-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 100069593-A-T

http://identifiers.org/hco/12/GRCh38#50696028-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#100069676-C-A

50696028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100069676-C-T

http://identifiers.org/hco/12/GRCh38#50696030-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#100069678-C-A

50696030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100069678-C-T

50696034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100069686-G-A

50696034-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100069686-G-T

http://identifiers.org/hco/12/GRCh38#50696070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#100069722-C-A

50696070-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100069722-C-G

50696070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100069722-C-T

50696842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100070915-A-G

50696930-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100070986-G-C

50696930-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100070986-G-T

http://identifiers.org/hco/12/GRCh38#50697029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#100071065-C-A

50697190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100071226-G-A

50697190-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100071226-G-T

50697245-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100071285-G-C

50697245-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100071285-G-T

50697331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100071386-C-T

50697351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100071406-C-T

50697497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100071519-A-G

50698285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100072258-G-A

50698285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100072258-G-T

http://identifiers.org/hco/12/GRCh38#50698615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#100072699-C-A

50698615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100072699-C-T

50698653-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100072736-C-G

50698679-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100072763-C-G

50698679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100072763-C-T

50698791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100072846-G-A

http://identifiers.org/hco/12/GRCh38#50699111-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#100073127-A-C

50699111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 100073127-A-G

http://identifiers.org/hco/12/GRCh38#50699262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#100073268-C-A

50699262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100073268-C-T

50699297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100073316-T-C

50703978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100075969-C-T

50704085-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100076269-C-G

50704085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100076269-C-T

50704090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100076274-A-G

50704105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100076288-G-A

50704180-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 100076363-T-G

50704275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100076459-T-C

http://identifiers.org/hco/12/GRCh38#50704307-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#100076491-C-A

50704580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100076845-A-G

50704979-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100077484-T-A

50704979-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100077484-T-G

50705072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100077574-G-A

50705178-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100077662-T-A

50705413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100077834-G-A

http://identifiers.org/hco/12/GRCh38#50705431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#100077852-C-A

50705695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100078247-C-T

50705863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100078415-G-A

50706326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100078764-C-T

50706327-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100078765-T-A

50706397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100078949-G-A

50706397-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100078949-G-T

50706426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100079002-G-A

http://identifiers.org/hco/12/GRCh38#50706520-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#100079172-A-C

50706606-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 100079258-T-A

50706642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 100079294-A-G

50706651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 100079303-T-C

50706651-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 100079303-T-G

50706680-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100079332-A-T

50706786-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100079406-G-T

50706788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100079408-A-G

50706788-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100079408-A-T

50706952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100079505-G-A

50707481-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100080046-C-G

50707481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100080046-C-T

50707518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100080079-A-G

50707605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100080151-A-G

50708309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100080756-T-C

50708320-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100080766-T-G

http://identifiers.org/hco/12/GRCh38#50708324-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#100080770-C-A

50708324-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100080770-C-G

50708324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100080770-C-T

50708325-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100080771-T-G

50708333-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100080776-G-T

50708364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100080808-T-C

50708569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 100081009-A-G

50708853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100081549-A-G

50709018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100081694-G-A

50714379-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100084009-G-C

50714379-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100084009-G-T

http://identifiers.org/hco/12/GRCh38#50714634-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#100084259-C-A

50714660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100084285-G-T

50718497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100087751-T-C

50718845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100088036-T-C

50718896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100088077-A-G

50718904-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100088085-A-T

http://identifiers.org/hco/12/GRCh38#50718945-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#100088127-A-C

50718945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100088127-A-G

50721202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100088798-A-G

50721230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100088826-C-T

50721419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100089014-A-G

50721521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100089113-A-G

http://identifiers.org/hco/12/GRCh38#50723260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#100091779-C-A

50723260-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 100091779-C-G

50723260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 100091779-C-T

50723426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100091933-A-G

50723458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100091964-T-C

50724279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100093118-T-C

50724350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100093166-T-C

50724390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100093175-G-T

50724472-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100093250-C-G

50724512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100093289-A-G

http://identifiers.org/hco/12/GRCh38#50724637-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#100093391-C-A

50724637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100093391-C-T

50724649-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100093403-A-T

50724667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100093421-T-C

50724889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100093786-G-A

50726224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100095108-T-C

50726247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100095129-G-A

50727452-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100096576-G-C

http://identifiers.org/hco/12/GRCh38#50727568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#100096685-C-A

50727568-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100096685-C-G

http://identifiers.org/hco/12/GRCh38#50727655-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#100096775-A-C

50727655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100096775-A-G

50727659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100096779-T-C

50727659-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100096779-T-G

50727734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 100096853-G-A

50727743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 100096862-G-A

50727743-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 100096862-G-T

50727752-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 100096871-T-A

50727764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 100096883-A-G

50727858-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100096988-A-T

http://identifiers.org/hco/12/GRCh38#50727883-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#100097011-A-C

50727902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100097030-G-A

50727902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100097030-G-T

50728415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100097227-G-A

50728415-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100097227-G-T

50728683-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100097475-G-T

50728901-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100097673-A-G

50728933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100097704-T-C

50728933-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100097704-T-G

50731182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100099923-T-C

http://identifiers.org/hco/12/GRCh38#50731225-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#100099966-A-C

50731225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100099966-A-G

50731438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 100100138-C-T

50731450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 100100150-C-T

50731522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 100100222-A-G

50731608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100100305-C-T

50731634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100100329-G-A

50731634-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100100329-G-C

50731634-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100100329-G-T

http://identifiers.org/hco/12/GRCh38#50731907-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#100100561-A-C

50732267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100100949-G-A

50732380-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 100101027-C-G

50732380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 100101027-C-T

50732491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 100101138-C-T

50734111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100102940-A-G

50734111-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100102940-A-T

50734149-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 100102978-T-G

50734324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100103111-G-T

http://identifiers.org/hco/12/GRCh38#50734955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#100104181-C-A

50735190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100104379-A-G

50735353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100104505-C-T

50735359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100104511-T-C

50736115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100104782-G-A

50736272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100104897-C-T

50736579-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100105186-C-G

50736919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100105485-C-T

50736978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100105538-C-T

50737305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100105915-C-T

50739006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100106874-A-G

50739293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100107152-A-G

50739432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 100107483-A-G

50739706-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100107738-T-A

50739706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100107738-T-C

http://identifiers.org/hco/12/GRCh38#50739710-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#100107742-C-A

50739710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100107742-C-T

50739726-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100107761-T-A

50739735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100107770-G-T

http://identifiers.org/hco/12/GRCh38#50741337-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#100109796-C-A

50741337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100109796-C-T

http://identifiers.org/hco/12/GRCh38#50741368-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#100109827-C-A

50741368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100109827-C-T

50741420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 100109869-T-C

50741477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 100109926-A-G

50741558-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100110003-A-T

50741602-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100110046-A-T

50742593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100111465-T-C

50744746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 100113218-G-A

50744746-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 100113218-G-C

50744746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 100113218-G-T

50744758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 100113230-A-G

50744946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 100113383-A-G

50744974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 100113411-T-C

50745030-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100113467-G-T

http://identifiers.org/hco/12/GRCh38#50745215-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#100113647-C-A

50745215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100113647-C-T

http://identifiers.org/hco/12/GRCh38#50745243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#100113674-C-A

50745243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100113674-C-T

http://identifiers.org/hco/12/GRCh38#50745288-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#100113719-C-A

50745289-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100113720-T-A

50745362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100113784-G-T

50745582-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100113931-G-T

50745674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100114025-T-C

http://identifiers.org/hco/12/GRCh38#50745696-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#100114047-C-A

50745696-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100114047-C-G

50745729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100114073-A-G

50745741-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100114085-G-T

50745772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100114116-T-C

50745908-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100114236-G-C

50745908-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100114236-G-T

http://identifiers.org/hco/12/GRCh38#50746008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#100114318-C-A

http://identifiers.org/hco/12/GRCh38#50746538-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#100114830-C-A

50746539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100114831-T-C

50746544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100114835-G-A

50746632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100114910-A-G

50746632-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100114910-A-T

50746918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100115324-G-A

50746918-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100115324-G-C

http://identifiers.org/hco/12/GRCh38#50747271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#100115782-C-A

50747278-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100115789-A-T

http://identifiers.org/hco/12/GRCh38#50747340-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#100115992-C-A

50747565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100116198-G-A

50747565-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100116198-G-T

http://identifiers.org/hco/12/GRCh38#50747610-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#100116240-C-A

50747627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100116257-G-A

50747646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100116276-A-G

50747664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100116295-A-G

50747703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100116340-A-G

http://identifiers.org/hco/12/GRCh38#50747708-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#100116345-C-A

50747754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100116376-G-T

http://identifiers.org/hco/12/GRCh38#50747970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#100116722-C-A

50748180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29284
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100116883-T-C