32825424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 75174094-T-C

32826497-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75175186-T-G

32826515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75175204-C-T

32826534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75175245-G-A

32826664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75175374-G-A

http://identifiers.org/hco/2/GRCh38#32831056-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75176073-A-C

32831405-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75176395-T-A

32831423-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75176413-G-C

32831650-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75176579-G-C

32831669-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75176597-G-C

32831838-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75176764-G-T

http://identifiers.org/hco/2/GRCh38#32832170-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75177081-C-A

32832180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75177091-C-T

http://identifiers.org/hco/2/GRCh38#32832184-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75177095-A-C

32832238-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75177144-C-G

32832316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75177219-G-A

32832515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75177424-C-T

32832619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75177532-A-G

32832889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75177806-G-A

32832889-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75177806-G-T

32833428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75178223-A-G

32833428-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75178223-A-T

32833633-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75178304-A-G

32833694-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75178373-T-C

32833891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75178543-C-T

32833969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75178597-G-A

32834064-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75178682-T-G

32834635-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75179924-C-G

32834666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75179968-G-A

32834666-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75179968-G-T

32834671-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75179973-T-A

32834736-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75180034-T-G

32834747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75180044-A-G

32837050-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75182087-G-T

32837157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75182155-G-A

32837158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75182156-C-T

32837317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75182303-C-T

32837598-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75182683-G-C

32837915-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75182992-C-G

32837915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75182992-C-T

32839110-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75183722-G-C

32839166-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75183780-G-C

32839230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75183871-G-A

32839429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75184067-T-C

32839464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75184094-C-T

32839494-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75184118-T-A

32839597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75184223-A-G

32839825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75184795-A-G

32839828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75184798-G-A

32839909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75184880-T-C

32839914-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75184885-T-A

32840071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75185982-C-T

32840185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75186056-C-T

32840194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75186065-C-T

32840248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75186111-T-C

32840347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75186187-G-A

32840347-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75186187-G-T

32840349-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75186188-T-A

32840440-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75186279-C-G

32840635-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75186487-G-T

32840868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75186728-A-G

32840971-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75186823-A-T

http://identifiers.org/hco/2/GRCh38#32840975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75186827-C-A

32840975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75186827-C-T

32841006-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 75186855-T-G

32842118-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75187160-A-G

32842363-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75187426-G-C

http://identifiers.org/hco/2/GRCh38#32842465-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75187530-C-A

32842551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75187603-A-G

32842723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75187787-G-A

32842776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75187838-G-A

32842777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75187839-C-T

32842925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75188021-C-T

32843236-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75188477-T-G

32843255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75188496-A-G

32843259-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75188500-A-T

32843265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75188506-G-A

32843420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75188660-G-A

32843556-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75188789-G-T

32843643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75188880-A-G

32844048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75189218-C-T

32846751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75189485-G-T

http://identifiers.org/hco/2/GRCh38#32846929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75189686-C-A

32847001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75189772-G-A

32847708-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75189938-T-G

http://identifiers.org/hco/2/GRCh38#32847746-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75189976-C-A

32847746-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75189976-C-G

32847919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75190147-C-T

32848094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75190315-T-C

http://identifiers.org/hco/2/GRCh38#32848113-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75190334-A-C

32848113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75190334-A-G

32848190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75190390-T-C

http://identifiers.org/hco/2/GRCh38#32848217-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75190417-A-C

32848676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75190483-C-T

32848678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75190490-G-A

32848942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75190691-G-A

32849071-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75190804-C-G

32849116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75190830-G-A

32849144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75190858-C-T

32849196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75190889-C-T

32849366-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75191040-T-G

32849864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75191377-G-A

32849933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75191421-A-G

32850034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75191521-C-T

http://identifiers.org/hco/2/GRCh38#32850091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75191580-C-A

32850362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75191818-A-G

32850377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75191833-C-T

32850378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75191834-G-A

32851525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75192642-G-A

32851534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75192651-A-G

32851614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75192729-A-G

32851771-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75192865-T-A

32851874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75192973-T-C

32851917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75193016-C-T

32851921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75193020-G-A

32852103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75193190-A-G

32852129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75193216-T-C

32852257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75193358-A-G

http://identifiers.org/hco/2/GRCh38#32852827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75194021-C-A

32852928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75194129-G-A

32852991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75194192-T-C

32853038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75194239-C-T

32853086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75194286-C-T

32853293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75194475-G-A

32853293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75194475-G-T

http://identifiers.org/hco/2/GRCh38#32853296-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75194478-C-A

32855859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75195461-C-T

32855903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75195523-A-G

32855934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75195564-T-C

32855940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75195570-G-A

32855968-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75195598-T-A

32856086-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75195713-A-T

32856301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75196306-T-C

32856378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75196360-G-A

http://identifiers.org/hco/2/GRCh38#32856430-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75196413-C-A

32856644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75196622-G-A

32856644-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75196622-G-C

32856697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75196677-G-A

32857003-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75196978-C-G

32857076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75197052-A-G

32857095-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75197071-T-G

http://identifiers.org/hco/2/GRCh38#32857231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75197175-C-A

32857231-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75197175-C-G

32857684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75210280-G-A

32857762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75210352-A-G

32857904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75210493-T-C

http://identifiers.org/hco/2/GRCh38#32857999-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75210571-A-C

32858202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75210768-A-G

32858214-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75210780-T-A

32858214-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75210780-T-G

32858228-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75210786-G-T

32863243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75236226-C-T

32863475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75236461-A-G

32863476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75236462-T-C

32863512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75236490-A-G

32863642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75236612-A-G

32863678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75236648-G-A

32863773-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75236750-G-C

32863897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75236836-G-A

32863951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75236877-C-T

32863986-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75236906-G-T

32864148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75237067-A-G

32864186-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75237107-A-T

32864208-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75237153-C-G

http://identifiers.org/hco/2/GRCh38#32864246-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75237198-A-C

32864264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75237216-T-C

32864268-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75237220-G-T

32864370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75237312-G-T

32864450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75237391-C-T

32864485-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75237421-T-A

32864539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75237472-C-T

32864548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75237481-C-T

32864613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75237543-A-G

32865344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75238379-C-T

32865490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75238565-C-T

32865531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75238616-T-C

http://identifiers.org/hco/2/GRCh38#32865566-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75238651-A-C

32865749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75238837-A-G

32865758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75238846-G-A

32865784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75238872-A-G

http://identifiers.org/hco/2/GRCh38#32865853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75238942-C-A

32865983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75239086-A-G

http://identifiers.org/hco/2/GRCh38#32877257-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75246883-A-C

32877384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75246991-A-G

32877401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75247007-G-A

32877508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75247113-T-C

32877630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75247220-G-T

http://identifiers.org/hco/2/GRCh38#32878230-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75247826-C-A

32878242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75247838-G-A

32878619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75248228-A-G

32878649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75248258-A-G

32878893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75248513-C-T

32878898-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75248518-T-A

32878910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75248530-A-G

32879296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75248842-G-A

32879319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75248866-A-G

32879550-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75249098-A-G

32879612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75249162-G-A

32882283-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75249454-C-G

http://identifiers.org/hco/2/GRCh38#32882665-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75249695-C-A

32882680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75249710-T-C

32882680-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75249710-T-G

32882711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75249738-C-T

32882727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75249754-G-A

http://identifiers.org/hco/2/GRCh38#32882738-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75249766-C-A

32882738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75249766-C-T

http://identifiers.org/hco/2/GRCh38#32882784-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75249806-A-C

32882831-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75249854-G-T

http://identifiers.org/hco/2/GRCh38#32882895-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75249917-C-A

32882895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75249917-C-T

32882919-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 75249946-G-T

32882961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75249981-G-A

32882982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75250002-T-C

32883107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75250123-C-T

32883218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75250233-G-A

32883329-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75250354-G-C

http://identifiers.org/hco/2/GRCh38#32883589-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75250587-A-C

32883589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75250587-A-G

32883735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75250740-A-G

32883793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75250784-G-A

32883801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75250790-C-T

32892215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75259204-G-A

32892298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75259298-A-G

32892298-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75259298-A-T

32892481-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75259463-A-T

32892718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75259725-T-C

32892756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75259751-A-G

32892760-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75259755-A-T

http://identifiers.org/hco/2/GRCh38#32892842-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75259841-A-C

32892862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75259866-G-A

32893052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75260034-C-T

32893085-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75260056-C-G

32893122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75260088-T-C

32893153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75260119-G-A

32894255-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75261351-T-G

32896341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75264404-T-C

32896346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75264409-T-C

32896384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75264445-G-T

32896445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75264504-G-T

32896567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75264613-C-T

http://identifiers.org/hco/2/GRCh38#32897633-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75266816-C-A

32897790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75266981-G-A

32898035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75267221-T-C

32898056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75267242-G-A

32898257-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75267446-G-C

32898273-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75267462-G-T

32898277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75267466-T-C

http://identifiers.org/hco/2/GRCh38#32898292-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75267490-A-C

32898440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75267637-C-T

http://identifiers.org/hco/2/GRCh38#32898537-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75267728-C-A

32898537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 75267728-C-T

32898558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75267749-G-T

http://identifiers.org/hco/2/GRCh38#32898559-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75267750-C-A

32898559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75267750-C-T

32898569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75267760-A-G

32898619-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75267812-T-A

32898633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75267826-T-C

32898715-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75267907-C-G

32899001-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75268179-C-G

32899212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75268388-C-T

32902621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75273905-C-T

32902622-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75273906-C-G

32902801-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75274094-T-G

32902971-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75274236-T-A

32903165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75274365-T-C

32903283-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75274485-T-G

32903308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75274510-G-A

32903522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75274732-T-C

32904349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75274917-G-A

32904570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75275140-A-G

32904786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75275336-A-G

32904832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75275380-C-T

32904947-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75275479-G-C

32905020-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75275548-T-G

http://identifiers.org/hco/2/GRCh38#32905031-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75275575-A-C

32905034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75275578-A-G

32905124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75275663-A-G

32905167-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75275706-G-C

32905233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75275780-A-G

32905448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75275982-C-T

32905571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75276124-T-C

32905656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75276216-A-G

32905664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75276224-A-G

http://identifiers.org/hco/2/GRCh38#32908963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75281918-C-A

32909186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75282112-T-C

32909361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75282278-T-C

32909401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75282319-A-G

32909420-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75282338-G-C

32909420-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75282338-G-T

32909586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75282517-A-G

32909606-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75282537-A-T

32909648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75282579-C-T

32909748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75282668-T-C

32910399-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75282860-G-C

32910403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75282864-G-A

32910624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75283057-A-G

32910636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75283069-G-A

32910689-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75283123-G-T

32910744-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75283180-G-T

32911148-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75283570-G-T

32911182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75283604-C-T

32918417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75285131-C-T

http://identifiers.org/hco/2/GRCh38#32918585-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75285267-A-C

32918585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75285267-A-G

32918585-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75285267-A-T

http://identifiers.org/hco/2/GRCh38#32918605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75285287-C-A

32918605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75285287-C-T

32918650-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75285325-G-T

32918849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75285513-A-G

32918892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75285556-A-G

32919256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75286861-G-A

32919427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75287013-C-T

32920174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75287136-G-A

32920677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75287194-C-T

32920725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75287250-T-C

32920794-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75287321-T-A

32920805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75287331-C-T

32920845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75287369-C-T

32920904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75287498-C-T

http://identifiers.org/hco/2/GRCh38#32922812-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75288113-A-C

32922907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75288209-G-A

32922907-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75288209-G-T

32923051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75288350-G-T

32923064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75288363-T-C

32923147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75289007-C-T

32923385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75289246-G-A

32923425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75289284-A-G

32923461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75289317-A-G

32923473-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75289329-G-C

32923709-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75289804-G-T

32923711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75289806-A-G

32923769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75289846-A-G

32923804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75289883-G-A

32923866-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75289956-G-C

32923870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75289960-C-T

32923931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75290021-G-A

32924760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75290359-G-A

32924803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75290403-G-A

32924806-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75290406-G-C

32925309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75290596-T-C

32925403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: non coding transcript exon variant
orthologous variants: 75290696-T-C

32925460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: non coding transcript exon variant
orthologous variants: 75290744-C-T

http://identifiers.org/hco/2/GRCh38#32925482-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75290752-C-A

http://identifiers.org/hco/2/GRCh38#32925611-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75290871-C-A

32925611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: non coding transcript exon variant
orthologous variants: 75290871-C-T

32925775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: non coding transcript exon variant
orthologous variants: 75291475-G-A

32925789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: non coding transcript exon variant
orthologous variants: 75291489-C-T

32925800-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: non coding transcript exon variant
orthologous variants: 75291500-G-T

32925894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: non coding transcript exon variant
orthologous variants: 75291597-G-A

32925894-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: non coding transcript exon variant
orthologous variants: 75291597-G-C

32925894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: non coding transcript exon variant
orthologous variants: 75291597-G-T

32925932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: non coding transcript exon variant
orthologous variants: 75291634-G-T

32926059-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: non coding transcript exon variant
orthologous variants: 75291754-T-G

http://identifiers.org/hco/2/GRCh38#32926070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75291764-C-A

http://identifiers.org/hco/2/GRCh38#32926161-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75291853-C-A

32926165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: non coding transcript exon variant
orthologous variants: 75291857-C-T

http://identifiers.org/hco/2/GRCh38#32926334-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75292018-A-C

32926334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: non coding transcript exon variant
orthologous variants: 75292018-A-G

32926440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: non coding transcript exon variant
orthologous variants: 75292096-A-G

http://identifiers.org/hco/2/GRCh38#32926442-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75292098-C-A

32926442-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: non coding transcript exon variant
orthologous variants: 75292098-C-G

32926477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: non coding transcript exon variant
orthologous variants: 75292137-G-A

32926497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: non coding transcript exon variant
orthologous variants: 75292157-C-T

32926619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: non coding transcript exon variant
orthologous variants: 75292199-G-A

32926619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42946
most severe consequence: non coding transcript exon variant
orthologous variants: 75292199-G-T