67448474-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 78989501-G-C

http://identifiers.org/hco/14/GRCh38#67448998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#78989910-C-A

67448998-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 78989910-C-G

67448998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 78989910-C-T

67452815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 78990662-C-T

67452922-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 78990793-T-A

67452925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 78990796-T-C

67453460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 78991475-G-A

67453487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 78991502-C-T

67453611-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 78991624-G-C

67453650-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 78991660-T-G

67453895-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 78991912-T-A

67454098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 78992271-G-A

67454234-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 78992426-T-A

67454234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 78992426-T-C

67454329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 78992501-T-C

67454520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 78992741-A-G

67454583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 78992753-A-G

http://identifiers.org/hco/14/GRCh38#67454772-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#78992901-C-A

67454772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78992901-C-T

67455139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78993032-T-C

67455185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78993073-T-C

http://identifiers.org/hco/14/GRCh38#67455240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#78993131-C-A

67455240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78993131-C-T

http://identifiers.org/hco/14/GRCh38#67455312-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#78993193-A-C

67455379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78993259-G-A

67455520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78993429-A-G

http://identifiers.org/hco/14/GRCh38#67455590-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#78993484-A-C

67455839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78993728-T-C

http://identifiers.org/hco/14/GRCh38#67455843-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#78993732-C-A

67457988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78994487-C-T

67458043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78994544-G-A

67458043-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78994544-G-C

http://identifiers.org/hco/14/GRCh38#67458156-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#78994664-C-A

67458156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78994664-C-T

67458181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78994689-G-A

67458181-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78994689-G-C

67458194-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78994702-A-T

67458293-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78994799-T-A

67458293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78994799-T-C

67458420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78994926-C-T

67458422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78994928-G-T

67458497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78994992-G-A

67458696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78995185-C-T

67458885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78995368-T-C

http://identifiers.org/hco/14/GRCh38#67459107-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#78996631-C-A

67459658-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78997132-G-C

67459674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78997148-T-C

67459739-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78997209-A-T

67459774-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78997246-T-A

67459774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78997246-T-C

67460299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78998174-G-A

67460471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78998310-G-A

67460558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78998418-G-A

67460673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78998519-C-T

67461370-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78999033-G-C

67461483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78999135-G-A

67461526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78999172-C-T

67461639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78999287-G-A

67461795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78999448-G-A

67461941-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78999583-T-A

67462681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79003090-C-T

67463884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79004080-T-C

67464047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79004234-G-A

67464067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79004247-T-C

67464112-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79004261-G-T

http://identifiers.org/hco/14/GRCh38#67464125-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#79004274-C-A

67464154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79004292-C-T

67464267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79004407-G-A

67464267-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79004407-G-C

67464367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79004505-C-T

67466207-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79004870-T-G

67466237-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79004899-G-T

67466238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79004900-C-T

67466391-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79005022-A-T

67466463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79005095-T-C

http://identifiers.org/hco/14/GRCh38#67466804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#79005303-C-A

67467033-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79005464-T-G

67467124-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79005535-G-T

67467175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79005587-A-G

http://identifiers.org/hco/14/GRCh38#67467180-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#79005592-C-A

67467180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79005592-C-T

67467210-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79005633-A-T

67467296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79005717-A-G

http://identifiers.org/hco/14/GRCh38#67467302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#79005723-C-A

67467302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79005723-C-T

http://identifiers.org/hco/14/GRCh38#67467371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#79005791-C-A

67467371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79005791-C-T

67467464-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79005875-A-T

67467479-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79005885-A-T

http://identifiers.org/hco/14/GRCh38#67467618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#79006016-C-A

67467621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79006019-C-T

http://identifiers.org/hco/14/GRCh38#67467705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#79006090-C-A

67468395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79006664-G-A

67468616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79006846-G-A

67468682-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79006895-T-G

67468709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79006943-C-T

67469283-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79007907-G-C

67469755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79008137-G-A

67469764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79008146-G-A

67469944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79008310-C-T

67470121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79008429-T-C

67470122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79008430-G-A

67470122-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79008430-G-C

67470183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79008491-A-G

http://identifiers.org/hco/14/GRCh38#67470333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#79008632-C-A

67470333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79008632-C-T

67470353-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79008650-T-A

67470371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79008668-G-A

67470371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79008668-G-T

67470392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79008689-C-T

http://identifiers.org/hco/14/GRCh38#67470426-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#79008723-C-A

67470426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79008723-C-T

67470513-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79008811-G-T

67470521-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79008819-C-G

67470521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79008819-C-T

67470543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79008837-G-T

http://identifiers.org/hco/14/GRCh38#67470596-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#79008890-C-A

67470596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79008890-C-T

67470637-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79008927-G-T

http://identifiers.org/hco/14/GRCh38#67470642-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#79008932-C-A

67470642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79008932-C-T

67470848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79009116-G-A

67470929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79009188-C-T

67470980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79009241-A-G

67470995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79009256-T-C

67470996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79009257-G-A

67470996-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79009257-G-C

67471011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79009272-T-C

67471013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79009274-T-C

http://identifiers.org/hco/14/GRCh38#67471030-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#79009290-C-A

67471030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79009290-C-T

67471042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79009302-G-A

67471042-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79009302-G-T

http://identifiers.org/hco/14/GRCh38#67471048-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#79009308-C-A

67471231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79009489-A-G

http://identifiers.org/hco/14/GRCh38#67471271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#79009528-C-A

67471306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79009555-G-T

67471313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79009562-G-A

67471380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79009597-G-A

67471381-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79009598-C-G

67471381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79009598-C-T

http://identifiers.org/hco/14/GRCh38#67471426-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#79009639-C-A

67471426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79009639-C-T

67471517-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79009687-A-T

http://identifiers.org/hco/14/GRCh38#67471534-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#79009704-C-A

67471534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79009704-C-T

http://identifiers.org/hco/14/GRCh38#67471535-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#79009705-C-A

67471578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79009734-G-T

67471629-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79009781-G-T

67471651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79009792-T-C

67471654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79009795-G-A

67471654-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79009795-G-T

67471726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79009869-A-G

http://identifiers.org/hco/14/GRCh38#67471793-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#79009910-C-A

67471793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79009910-C-T

67471832-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79009937-C-G

67471832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79009937-C-T

67471854-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79009961-A-T

67471860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79009967-G-A

67471929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79010021-C-T

67471944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79010036-T-C

67471957-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79010049-G-C

67471957-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79010049-G-T

67472023-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79010109-G-T

67472111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79010193-G-A

67472111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79010193-G-T

67472121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79010202-G-T

67472126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79010207-G-T

67472198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79010271-T-C

67472263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79010323-T-C

67472274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79010334-A-G

67472364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79010403-A-G

67472389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79010427-C-T

67472514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79010527-C-T

67472580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79010580-G-A

67472580-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79010580-G-T

67472657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79010654-G-A

67472668-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79010667-G-T

67472746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79010746-G-A

67472746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79010746-G-T

http://identifiers.org/hco/14/GRCh38#67472759-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#79010759-C-A

67472759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79010759-C-T

http://identifiers.org/hco/14/GRCh38#67472879-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#79010885-C-A

67472879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79010885-C-T

http://identifiers.org/hco/14/GRCh38#67472917-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#79010924-C-A

67472917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79010924-C-T

67473030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79011036-A-G

http://identifiers.org/hco/14/GRCh38#67473045-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#79011051-A-C

http://identifiers.org/hco/14/GRCh38#67473101-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#79011133-A-C

67473101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79011133-A-G

67473101-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79011133-A-T

67473146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79011169-A-G

http://identifiers.org/hco/14/GRCh38#67473166-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#79011190-C-A

http://identifiers.org/hco/14/GRCh38#67473172-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#79011196-C-A

67473193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79011217-G-A

67473193-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79011217-G-C

67473193-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79011217-G-T

http://identifiers.org/hco/14/GRCh38#67473240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#79011256-C-A

67473240-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79011256-C-G

67473240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79011256-C-T

http://identifiers.org/hco/14/GRCh38#67473360-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#79011356-C-A

67473360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79011356-C-T

67473386-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79011391-T-A

67473386-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79011391-T-C

67473386-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79011391-T-G

67473387-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79011392-G-T

http://identifiers.org/hco/14/GRCh38#67473397-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#79011402-C-A

67473441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 79011447-G-A

http://identifiers.org/hco/14/GRCh38#67473468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#79011474-C-A

67473468-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 79011474-C-G

67473651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 79011657-G-A

67473651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 79011657-G-T

http://identifiers.org/hco/14/GRCh38#67473666-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#79011672-C-A

67473697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 79011703-C-T

67473786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 79011792-G-A

http://identifiers.org/hco/14/GRCh38#67473837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#79011843-C-A

67473837-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 79011843-C-G

67473837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 79011843-C-T

67473849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 79011855-C-T

http://identifiers.org/hco/14/GRCh38#67473909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#79011915-C-A

67473909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 79011915-C-T

67473912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 79011918-G-A

67473912-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 79011918-G-C

67473912-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 79011918-G-T

67473937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, splice_region_variant
orthologous variants: 79011943-G-A

67473937-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, splice_region_variant
orthologous variants: 79011943-G-C

67473937-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, splice_region_variant
orthologous variants: 79011943-G-T

67473970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79011975-G-A

67473970-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79011975-G-T

67475795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79014790-T-C

67475818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79014813-C-T

67477263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79015881-G-A

http://identifiers.org/hco/14/GRCh38#67477367-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#79015962-A-C

http://identifiers.org/hco/14/GRCh38#67477384-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#79015980-C-A

67477446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79016036-T-C

67477577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79016137-C-T

67478131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79016619-G-A

67478432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79017469-A-G

67478806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79017836-C-T

67478878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79017909-C-T

67478998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79018009-C-T

67480334-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 79018659-C-G

67480649-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79018956-C-G

67481346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79019675-C-T

67481659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79019924-A-G

http://identifiers.org/hco/14/GRCh38#67481751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#79020016-C-A

http://identifiers.org/hco/14/GRCh38#67481775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#79020039-C-A

67481940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79020157-G-A

http://identifiers.org/hco/14/GRCh38#67482402-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#79020724-C-A

http://identifiers.org/hco/14/GRCh38#67482571-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#79020846-C-A

http://identifiers.org/hco/14/GRCh38#67482795-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#79021109-A-C

http://identifiers.org/hco/14/GRCh38#67482835-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#79021147-C-A

67482860-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79021169-C-G

67482890-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79021196-G-C

67482975-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79021269-G-T

67483546-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79021514-T-A

67483808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79021803-G-T

67483936-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79021937-T-A

67483995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79021997-G-A

67483998-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79022000-G-C

http://identifiers.org/hco/14/GRCh38#67484122-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#79022289-C-A

67484934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79022948-G-A

http://identifiers.org/hco/14/GRCh38#67484991-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#79023005-A-C

67485654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79023988-C-T

67486935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79024469-G-A

http://identifiers.org/hco/14/GRCh38#67486944-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#79024478-C-A

67486944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79024478-C-T

67487017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 79024552-G-A

67487017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 79024552-G-T

67487090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 79024633-T-C

http://identifiers.org/hco/14/GRCh38#67487111-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#79024654-C-A

http://identifiers.org/hco/14/GRCh38#67487121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#79024664-C-A

67487121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79024664-C-T

67487149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79024692-G-A

67487149-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79024692-G-T

67487193-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79024736-T-A

67487239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79024788-A-G

http://identifiers.org/hco/14/GRCh38#67487262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#79024811-C-A

67487262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79024811-C-T

http://identifiers.org/hco/14/GRCh38#67487552-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#79025079-A-C

67488079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79027019-C-T

67488213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 79027102-T-C

67488222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 79027111-C-T

67488371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 79027251-G-T

http://identifiers.org/hco/14/GRCh38#67488426-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#79027343-C-A

67488426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79027343-C-T

67488443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 79027360-G-A

67488443-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 79027360-G-T

http://identifiers.org/hco/14/GRCh38#67488467-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#79027383-C-A

67488467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 79027383-C-T

http://identifiers.org/hco/14/GRCh38#67488503-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#79027418-C-A

67488503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79027418-C-T

http://identifiers.org/hco/14/GRCh38#67488514-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#79027429-C-A

67488514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 79027429-C-T

67488529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 79027444-A-G

67488529-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 79027444-A-T

67488548-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 79027467-T-C

http://identifiers.org/hco/14/GRCh38#67488585-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#79027504-C-A

67488585-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 79027504-C-G

67488585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 79027504-C-T

67488697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 79027612-C-T

67489001-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 79027901-T-G

67489105-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79028209-C-G

67489508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79028655-C-T

67489525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79028672-T-C

67490218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79029025-G-T

67490236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79029050-C-T

67490441-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79029241-T-C

67490552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79029335-G-A

67490552-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79029335-G-C

67490659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79029448-T-C

67490825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79029591-A-G

67490890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79029895-G-A

http://identifiers.org/hco/14/GRCh38#67490892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#79029897-C-A

67490892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79029897-C-T

67490946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79029937-C-T

http://identifiers.org/hco/14/GRCh38#67492196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#79030896-C-A

67492196-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79030896-C-G

67492196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79030896-C-T

http://identifiers.org/hco/14/GRCh38#67492296-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#79031002-C-A

67494148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79034513-A-G

67494338-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79034703-C-G

67494338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79034703-C-T

67495416-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79036485-T-A

67496014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79036807-T-C

67496016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79036809-G-A

67496030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79036823-C-T

67499320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79040602-T-C

67499398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79040665-T-C

67499536-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79040803-G-C

67499621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79040888-G-A

67499714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79040988-T-C

67499715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79040989-A-G

67499726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79041000-G-A

67499727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79041001-C-T

67499795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79041065-C-T

67500252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79041485-G-A

67501539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79042230-G-A

67501539-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79042230-G-T

67502868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79042894-A-G

67502969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79043105-T-C

67503224-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79043318-G-C

67503363-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79043415-G-T

67503381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79043433-A-G

67503417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79043465-G-A

67503498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79043538-G-A

67503498-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79043538-G-T

67503628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79043690-T-C

http://identifiers.org/hco/14/GRCh38#67505339-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#79044774-A-C

67505471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79044885-T-C

67505637-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79045025-G-C

67505847-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79045236-C-G

67506326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79045523-T-C

67506469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79045618-G-A

67506562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79046340-G-A

67508152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79046918-G-A

67508152-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79046918-G-C

67508156-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79046922-T-A

67508257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79047022-C-T

67508321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79047085-C-T

67508650-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79047396-G-T

67509009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79047701-G-A

67509163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79047794-C-T

67509284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79048318-C-T

67510390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79048785-G-A

67510401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79048797-C-T

67510599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79048991-C-T

67510603-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79048995-G-C

http://identifiers.org/hco/14/GRCh38#67511117-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#79049683-A-C

67511117-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79049683-A-T

67511433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79050037-G-A

http://identifiers.org/hco/14/GRCh38#67511505-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#79050110-C-A

http://identifiers.org/hco/14/GRCh38#67511652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#79050215-C-A

67511652-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79050215-C-G

67511652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79050215-C-T

67511710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79050259-G-A

67511710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79050259-G-T

67511743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79050292-C-T

67511844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79050384-T-C

67512840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79051505-G-A

http://identifiers.org/hco/14/GRCh38#67512919-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#79051587-A-C

67512968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79051636-A-G

67513204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79051868-G-A

67513204-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79051868-G-C

67513254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79051918-A-G

67513315-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79051961-T-A

67513375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79052021-T-C

67513463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79052112-G-A

67513944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79052592-C-T

67514075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79052792-G-A

67514100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79052817-G-A

67514120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79052836-C-T

67514163-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79052867-G-C

67514215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79052901-C-T

67514271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79052960-G-A

67514271-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79052960-G-T

67514342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79053019-G-T

67514500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79053165-C-T

67514695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79053340-G-A

67514885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79053546-G-A

67514887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79053548-C-T

67514903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79053564-G-A

67515013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79053674-G-A

67515013-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79053674-G-C

67515013-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79053674-G-T

67515075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79053736-G-T

67515094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79053755-G-A

67515094-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79053755-G-T

67515104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79053765-G-A

67515104-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79053765-G-T

67515170-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79053839-G-T

http://identifiers.org/hco/14/GRCh38#67515285-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#79053953-C-A

67515285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 79053953-C-T

67515370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 79054028-G-A

67515370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 79054028-G-T

67515430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79054072-G-A

67515430-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79054072-G-T

67515457-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 79054099-T-A

67515457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 79054099-T-C

http://identifiers.org/hco/14/GRCh38#67515511-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#79054153-C-A

67515511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron variant
orthologous variants: 79054153-C-T

67515538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron variant
orthologous variants: 79054180-G-A

67515538-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron variant
orthologous variants: 79054180-G-T

http://identifiers.org/hco/14/GRCh38#67515563-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#79054205-C-A

67515563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron_variant, undefined
orthologous variants: 79054205-C-T

67515609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron_variant, undefined
orthologous variants: 79054261-G-A

67515798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron_variant, undefined
orthologous variants: 79054445-C-T

67515818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron_variant, undefined
orthologous variants: 79054465-A-G

http://identifiers.org/hco/14/GRCh38#67516233-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#79054907-C-A

67516235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron variant
orthologous variants: 79054909-G-A

67516337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron variant
orthologous variants: 79055471-C-T

67516346-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron variant
orthologous variants: 79055480-T-G

67516377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron variant
orthologous variants: 79055511-C-T

67516443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron variant
orthologous variants: 79056664-T-C

67517080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron variant
orthologous variants: 79057343-G-A

67517452-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron variant
orthologous variants: 79057686-C-G

67517612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron variant
orthologous variants: 79057826-C-T

67518043-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron variant
orthologous variants: 79058229-G-T

67518197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron variant
orthologous variants: 79058387-G-A

67518483-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron variant
orthologous variants: 79059123-A-T

67518646-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron variant
orthologous variants: 79059431-A-T

67518677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron variant
orthologous variants: 79059461-C-T

67520754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron variant
orthologous variants: 79061619-T-C

67520828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron variant
orthologous variants: 79061695-C-T

67521140-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron variant
orthologous variants: 79061939-T-G

67521687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron variant
orthologous variants: 79062563-A-G

67522360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron variant
orthologous variants: 79062996-G-A

67522384-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron variant
orthologous variants: 79063020-C-G

67522585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron variant
orthologous variants: 79063225-C-T

http://identifiers.org/hco/14/GRCh38#67522609-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#79063249-A-C

67522667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron variant
orthologous variants: 79063329-C-T

67522871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron variant
orthologous variants: 79063541-G-A

67522895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron variant
orthologous variants: 79063552-T-C

67523643-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron variant
orthologous variants: 79063913-T-A

67523853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron variant
orthologous variants: 79064123-A-G

67523853-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron variant
orthologous variants: 79064123-A-T

67523962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron variant
orthologous variants: 79064225-T-C

67523962-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron variant
orthologous variants: 79064225-T-G

67523963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron variant
orthologous variants: 79064226-G-A

67523989-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron variant
orthologous variants: 79064251-T-G

67524461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron variant
orthologous variants: 79064813-A-G

67524635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron variant
orthologous variants: 79064991-G-A

http://identifiers.org/hco/14/GRCh38#67524710-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#79065066-C-A

67524710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron_variant, undefined
orthologous variants: 79065066-C-T

67524722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron variant
orthologous variants: 79065078-A-G

67525197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron variant
orthologous variants: 79065534-G-A

67525608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron variant
orthologous variants: 79066887-A-G

67525751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron variant
orthologous variants: 79067029-G-A

67525766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron variant
orthologous variants: 79067044-C-T

67525903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron variant
orthologous variants: 79067180-A-G

67526007-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron variant
orthologous variants: 79067272-G-C

http://identifiers.org/hco/14/GRCh38#67526597-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#79069656-A-C

67526604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron variant
orthologous variants: 79069663-A-G

67526737-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron variant
orthologous variants: 79069797-G-T

67526825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron variant
orthologous variants: 79069879-T-C

67527085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron_variant, undefined
orthologous variants: 79070013-T-C

67527528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron variant
orthologous variants: 79070390-A-G

67527545-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron variant
orthologous variants: 79070407-G-T

67527894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron variant
orthologous variants: 79070731-A-G

67528295-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron variant
orthologous variants: 79071101-G-T

67528395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron variant
orthologous variants: 79071188-C-T

67528586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron variant
orthologous variants: 79071311-T-C

http://identifiers.org/hco/14/GRCh38#67528714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#79071408-C-A

67528717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron variant
orthologous variants: 79071411-G-A

67528717-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron variant
orthologous variants: 79071411-G-C

67529134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron variant
orthologous variants: 79071871-C-T

67529326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron variant
orthologous variants: 79072020-T-C

67529613-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron variant
orthologous variants: 79072254-T-G

http://identifiers.org/hco/14/GRCh38#67529654-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#79072318-C-A

67529813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron variant
orthologous variants: 79072424-G-T

67530527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron variant
orthologous variants: 79073707-T-C

67530777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron variant
orthologous variants: 79073951-C-T

67530795-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron variant
orthologous variants: 79073969-T-G

67530865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron variant
orthologous variants: 79074038-T-C

http://identifiers.org/hco/14/GRCh38#67530941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#79074120-C-A

67530941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron variant
orthologous variants: 79074120-C-T

67532186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron variant
orthologous variants: 79075059-A-G

67532735-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron variant
orthologous variants: 79075702-C-G

67532735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron variant
orthologous variants: 79075702-C-T

67532850-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron_variant, undefined
orthologous variants: 79075799-G-C

http://identifiers.org/hco/14/GRCh38#67532898-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#79075849-A-C

67532898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron_variant, undefined
orthologous variants: 79075849-A-G

67532899-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron variant
orthologous variants: 79075850-T-G

67533135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron variant
orthologous variants: 79075980-G-A

67533179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron variant
orthologous variants: 79075999-G-A

67533262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron_variant, undefined
orthologous variants: 79076076-G-A

67533262-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron_variant, undefined
orthologous variants: 79076076-G-C

67533301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 79076115-G-A

67533301-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 79076115-G-C

67533301-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 79076115-G-T

67533334-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 79076136-C-G

67533334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 79076136-C-T

http://identifiers.org/hco/14/GRCh38#67533344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#79076140-C-A

67533344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 79076140-C-T

http://identifiers.org/hco/14/GRCh38#67533446-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#79076235-C-A

67533446-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron_variant, undefined
orthologous variants: 79076235-C-G

67533446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron_variant, undefined
orthologous variants: 79076235-C-T

67533459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron_variant, undefined
orthologous variants: 79076248-C-T

67533467-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron_variant, undefined
orthologous variants: 79076256-G-T

67533568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron_variant, undefined
orthologous variants: 79076332-G-A

67533651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 79076416-G-T

http://identifiers.org/hco/14/GRCh38#67533668-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#79076433-C-A

67533668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 79076433-C-T

http://identifiers.org/hco/14/GRCh38#67533748-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#79076505-C-A

67533748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron variant
orthologous variants: 79076505-C-T

67533758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: intron variant
orthologous variants: 79076515-T-C

67533793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 79076552-T-C

http://identifiers.org/hco/14/GRCh38#67533805-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#79076564-C-A

67533805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 79076564-C-T

67533832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20130
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 79076591-A-G