42506780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121475721-A-G

42506806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121475748-A-G

42506824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121475760-T-C

42506916-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121475792-A-T

http://identifiers.org/hco/3/GRCh38#42506961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#121475833-C-A

42507158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121476017-G-A

42507239-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121476092-G-T

http://identifiers.org/hco/3/GRCh38#42507319-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#121476178-C-A

42507319-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121476178-C-G

http://identifiers.org/hco/3/GRCh38#42507389-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#121476247-C-A

42507389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121476247-C-T

42507441-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121476314-T-C

42507785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121476601-G-T

http://identifiers.org/hco/3/GRCh38#42507902-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#121477211-C-A

42507902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121477211-C-T

http://identifiers.org/hco/3/GRCh38#42507918-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#121477229-A-C

42507949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121477257-A-G

42507949-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121477257-A-T

42507950-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121477258-G-T

42508070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121477376-A-G

42508439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121477706-C-T

42508443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121477710-G-A

42509955-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121478487-C-G

42510189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121478715-C-T

42510470-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121479162-G-C

42510470-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121479162-G-T

42510543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121479235-A-G

42511143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121480402-C-T

42511474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121480718-A-G

42511580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121480829-T-C

42511591-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121480840-A-T

42511610-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121480858-G-T

42511617-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121480865-G-T

http://identifiers.org/hco/3/GRCh38#42511670-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#121480917-C-A

42511670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121480917-C-T

42512142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121481311-G-A

42512142-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121481311-G-T

42512155-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121481324-T-A

http://identifiers.org/hco/3/GRCh38#42512212-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#121481353-C-A

42512212-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121481353-C-G

42512212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121481353-C-T

42512329-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121481440-G-T

42512443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121481501-A-G

http://identifiers.org/hco/3/GRCh38#42512722-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#121481745-C-A

42512722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121481745-C-T

http://identifiers.org/hco/3/GRCh38#42512752-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#121481776-C-A

42512768-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121481792-G-C

42512768-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121481792-G-T

http://identifiers.org/hco/3/GRCh38#42512796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#121481820-C-A

42512831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121481855-G-A

42512831-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121481855-G-T

http://identifiers.org/hco/3/GRCh38#42512846-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#121481877-C-A

42512846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121481877-C-T

http://identifiers.org/hco/3/GRCh38#42512871-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#121481904-C-A

42512881-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121481910-G-T

http://identifiers.org/hco/3/GRCh38#42512916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#121481946-C-A

42512916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121481946-C-T

42513024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121482035-G-A

42513024-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121482035-G-T

http://identifiers.org/hco/3/GRCh38#42513047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#121482060-C-A

42513047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121482060-C-T

42513067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121482080-G-A

42513067-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121482080-G-C

42513067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121482080-G-T

42513075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121482090-G-A

42513075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121482090-G-T

42513096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121482119-T-C

http://identifiers.org/hco/3/GRCh38#42513197-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#121482217-A-C

42513197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121482217-A-G

42513304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121482316-G-A

42513304-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121482316-G-T

42513327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121482337-T-C

http://identifiers.org/hco/3/GRCh38#42513336-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#121482346-C-A

42513366-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121482373-T-A

http://identifiers.org/hco/3/GRCh38#42513376-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#121482383-C-A

42513432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121482418-G-A

http://identifiers.org/hco/3/GRCh38#42513516-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#121482474-C-A

42513516-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121482474-C-G

42513516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121482474-C-T

42513569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121482623-T-C

42513569-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121482623-T-G

42513629-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121482699-G-T

42513649-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121482741-G-T

42513701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121482817-C-T

42513753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121482869-G-A

42513904-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121483001-G-T

42513909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121483006-C-T

42513955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121483055-T-C

42513956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121483056-G-A

42514003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121483117-G-A

42514003-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121483117-G-C

42514003-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121483117-G-T

42514992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121483535-C-T

42515324-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121483798-C-G

42515357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121483831-G-A

42515580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121484051-C-T

42515651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121484124-G-T

42515691-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121484164-T-C

42515862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121484307-C-T

42515893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121484338-T-C

42516167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121484558-G-A

http://identifiers.org/hco/3/GRCh38#42516206-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#121484597-A-C

http://identifiers.org/hco/3/GRCh38#42516428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#121484764-C-A

42516428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121484764-C-T

http://identifiers.org/hco/3/GRCh38#42516444-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#121484779-C-A

42516444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121484779-C-T

42516456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121484791-G-A

42516456-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121484791-G-T

42516461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121484796-G-A

42516559-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121484904-G-C

42516559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121484904-G-T

42516579-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121484928-G-C

42516579-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121484928-G-T

42516734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121485121-T-C

42516757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121485148-A-G

42516850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121485227-G-T

42516927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121485296-A-G

42517064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121485414-G-A

42517069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121485419-A-G

42518174-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121486304-T-G

42518251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121486395-T-C

42518339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121486478-A-G

42518354-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121486493-A-T

42519074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121487008-A-G

42519074-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121487008-A-T

http://identifiers.org/hco/3/GRCh38#42519337-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#121487227-C-A

42519356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121487249-A-G

42519356-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121487249-A-T

42519383-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121487273-A-T

42519390-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 121487280-T-A

42519390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 121487280-T-C

42519401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121487291-T-C

42519401-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121487291-T-G

42519436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121487316-G-A

42519436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121487316-G-T

42519831-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121487636-G-C

42521292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121487918-G-A

42521292-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121487918-G-T

42521320-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121487953-G-T

42521404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121488033-G-A

42521404-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121488033-G-T

42521410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121488039-G-A

42521442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121488052-T-C

42521442-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121488052-T-G

42525905-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121489251-G-T

http://identifiers.org/hco/3/GRCh38#42527317-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#121489946-A-C

42527317-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121489946-A-T

42527367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121490003-A-G

http://identifiers.org/hco/3/GRCh38#42527382-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#121490020-C-A

42527382-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121490020-C-G

42527425-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121490063-C-G

42527425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121490063-C-T

42527491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121490129-G-A

42527512-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121490150-A-T

http://identifiers.org/hco/3/GRCh38#42527551-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#121490158-C-A

http://identifiers.org/hco/3/GRCh38#42527603-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#121490177-C-A

42527603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121490177-C-T

http://identifiers.org/hco/3/GRCh38#42527628-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#121490201-C-A

42527628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121490201-C-T

42527673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121490224-T-C

42527720-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121490258-G-C

42527720-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121490258-G-T

http://identifiers.org/hco/3/GRCh38#42527955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#121490427-C-A

42527955-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121490427-C-G

42527955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121490427-C-T

42528196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121490642-C-T

42528197-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121490643-C-G

42528197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121490643-C-T

http://identifiers.org/hco/3/GRCh38#42528222-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#121490668-C-A

42528222-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121490668-C-G

42528222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121490668-C-T

42528282-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121490723-T-A

42528282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121490723-T-C

42528282-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121490723-T-G

42528283-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121490724-G-T

42528284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121490725-G-A

42528284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121490725-G-T

http://identifiers.org/hco/3/GRCh38#42528332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#121490760-C-A

42528332-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121490760-C-G

42528337-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121490766-T-A

http://identifiers.org/hco/3/GRCh38#42528352-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#121490781-C-A

42529605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121491764-G-A

42529605-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121491764-G-T

42529621-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121491780-G-T

42529642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121491804-A-G

42529652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121491833-G-A

42529652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121491833-G-T

42529655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121491836-G-A

42529655-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121491836-G-T

42529818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121491964-C-T

http://identifiers.org/hco/3/GRCh38#42529819-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#121491965-C-A

42529819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121491965-C-T

http://identifiers.org/hco/3/GRCh38#42529857-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#121492002-C-A

42529857-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121492002-C-G

http://identifiers.org/hco/3/GRCh38#42529917-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#121492038-C-A

42530575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_donor_variant, undefined
orthologous variants: 121493395-A-G

42530575-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_donor_variant, undefined
orthologous variants: 121493395-A-T

http://identifiers.org/hco/3/GRCh38#42530637-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#121493457-C-A

42530637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121493457-C-T

42530645-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121493465-A-T

http://identifiers.org/hco/3/GRCh38#42531052-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#121493813-C-A

42531052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 121493813-C-T

42531074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121493835-G-T

42531095-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121493856-T-A

42531095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121493856-T-C

42531098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121493859-G-A

42531098-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121493859-G-T

http://identifiers.org/hco/3/GRCh38#42531124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#121493876-C-A

42531124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121493876-C-T

42531135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121493885-A-G

42531137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121493887-G-A

42531137-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121493887-G-T

42531146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 121493896-G-A

42531146-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 121493896-G-T

42531181-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121493932-T-A

42531181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121493932-T-C

http://identifiers.org/hco/3/GRCh38#42531205-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#121493956-C-A

http://identifiers.org/hco/3/GRCh38#42531256-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#121494004-C-A

42531256-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121494004-C-G

42531271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121494019-C-T

http://identifiers.org/hco/3/GRCh38#42531352-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#121494104-C-A

http://identifiers.org/hco/3/GRCh38#42531580-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#121494327-C-A

42531580-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121494327-C-G

42531580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121494327-C-T

42531639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121494385-T-C

42531689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121494436-G-A

42531689-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121494436-G-T

42531800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 121494515-C-T

42531860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121494578-C-T

42531876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 121494594-T-C

http://identifiers.org/hco/3/GRCh38#42532039-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#121494700-A-C

42532066-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121494727-G-C

42532066-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121494727-G-T

42532116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121494772-A-G

42532202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121494832-T-C

42532325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121494958-T-C

42532472-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121495084-G-T

http://identifiers.org/hco/3/GRCh38#42532559-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#121495150-C-A

42532559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121495150-C-T

http://identifiers.org/hco/3/GRCh38#42532568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#121495155-C-A

42532568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 121495155-C-T

http://identifiers.org/hco/3/GRCh38#42532626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#121495206-C-A

42532626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 121495206-C-T

42532665-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 121495241-G-T

42532676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 121495251-G-A

42532684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121495259-G-A

42532684-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121495259-G-T

http://identifiers.org/hco/3/GRCh38#42532693-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#121495268-A-C

42532772-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121495336-G-T

42532789-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121495353-T-A

42532789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121495353-T-C

42532822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121495383-T-C

http://identifiers.org/hco/3/GRCh38#42532855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#121495416-C-A

42532855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121495416-C-T

42532895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121495453-T-C

42532976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121495734-T-C

42532982-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121495740-G-T

42533065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121495950-G-A

42533065-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121495950-G-T

42533136-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121496018-G-C

42533196-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 121496059-G-T

http://identifiers.org/hco/3/GRCh38#42533233-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#121496102-C-A