48549648-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 96237979-T-A

48549680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96237938-A-G

48549854-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96237746-T-G

48549855-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96237745-T-G

48549891-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, undefined
orthologous variants: 96237711-T-A

48549891-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, undefined
orthologous variants: 96237711-T-G

48549919-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 96237678-T-G

http://identifiers.org/hco/17/GRCh38#48550094-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#96237485-C-A

48550094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96237485-C-T

48550105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96237474-T-C

http://identifiers.org/hco/17/GRCh38#48550169-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#96237407-A-C

48550169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96237407-A-G

48550651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96236909-G-A

48550651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96236909-G-T

48550662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96236898-G-A

48550662-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96236898-G-C

48550662-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96236898-G-T

48551037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 96236523-G-A

48551085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 96236475-G-A

48551085-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 96236475-G-C

48551092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 96236468-T-C

48551118-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 96236442-C-G

48551118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 96236442-C-T

http://identifiers.org/hco/17/GRCh38#48551139-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#96236421-C-A

48551139-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 96236421-C-G

48551139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 96236421-C-T

http://identifiers.org/hco/17/GRCh38#48551142-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#96236418-C-A

48551142-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 96236418-C-G

48551142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 96236418-C-T

http://identifiers.org/hco/17/GRCh38#48551337-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#96236205-C-A

48551337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96236205-C-T

48551643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96235885-C-T

48551843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96235701-G-A

48552326-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96235221-G-T

http://identifiers.org/hco/17/GRCh38#48552545-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#96235002-A-C

48552545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96235002-A-G

48552607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96234949-T-C

48552607-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96234949-T-G

48552792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96234705-T-C

48552792-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96234705-T-G

http://identifiers.org/hco/17/GRCh38#48552875-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#96234620-C-A

48552875-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96234620-C-G

48552890-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96234604-T-G

http://identifiers.org/hco/17/GRCh38#48553146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#96234346-C-A

48553146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96234346-C-T

http://identifiers.org/hco/17/GRCh38#48553190-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#96234327-C-A

48553227-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96234304-G-C

48553227-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96234304-G-T

http://identifiers.org/hco/17/GRCh38#48553410-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#96234127-C-A

48553410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96234127-C-T

http://identifiers.org/hco/17/GRCh38#48553411-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#96234126-C-A

48553493-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96234085-T-G

http://identifiers.org/hco/17/GRCh38#48554023-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#96233551-A-C

48554023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96233551-A-G

48554326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96233221-A-G

48554442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96233085-G-A

48554985-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96232559-T-A

48554985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96232559-T-C

http://identifiers.org/hco/17/GRCh38#48555341-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#96232173-A-C

48555341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96232173-A-G

48555341-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96232173-A-T

48555671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96231835-C-T

http://identifiers.org/hco/17/GRCh38#48555698-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#96231820-C-A

48555698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96231820-C-T

48555839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96231677-G-A

48556005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96231512-G-A

48556104-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96231428-C-G

48556174-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 96231351-A-T

48556175-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 96231350-A-T

48556298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 96231219-T-C

48556381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 96231139-G-A

48556382-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 96231138-A-T

48556392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 96231120-A-G

48556613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 96230945-G-A

48556717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 96230841-G-A

48556717-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 96230841-G-T

48556756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 96230802-T-C

48556910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 96230655-C-T

http://identifiers.org/hco/17/GRCh38#48556922-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#96230643-C-A

48557152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 96230378-G-A

48557185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 96230346-G-A

48557196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 96230340-A-G

48557243-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 96230275-G-C

48557676-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96229840-T-G

48558291-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96229326-G-C

48558362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96229268-G-T

48558571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96229132-G-A

48558577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96229126-G-A

48558780-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96228931-G-C

48558834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96228895-G-A

48559039-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96228751-A-T

48559214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96228569-C-T

48559437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96228376-T-C

48559438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96228375-G-T

48559479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96228334-T-C

http://identifiers.org/hco/17/GRCh38#48559564-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#96228262-C-A

48559564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96228262-C-T

http://identifiers.org/hco/17/GRCh38#48559571-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#96228255-C-A

48559628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96228185-T-C

48559683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96228121-C-T

48559757-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96228038-G-T

48559761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96228034-A-G

48559771-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96228020-G-T

http://identifiers.org/hco/17/GRCh38#48559825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#96227968-C-A

48559825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96227968-C-T

48559878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96227944-G-A

48559878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96227944-G-T

http://identifiers.org/hco/17/GRCh38#48559881-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#96227941-C-A

48559898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96227925-A-G

48559898-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96227925-A-T

48560042-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96227804-T-A

http://identifiers.org/hco/17/GRCh38#48560112-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#96227748-C-A

48560112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96227748-C-T

48560171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96227677-G-A

48560191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96227657-G-A

48560191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96227657-G-T

http://identifiers.org/hco/17/GRCh38#48560192-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#96227656-C-A

48560192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96227656-C-T

48560349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96227499-T-C

48560386-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96227462-T-C

48560568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96227308-G-A

48560766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96227099-G-A

48560790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96227075-T-C

48561539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96226672-C-T

48561607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96226605-A-G

48561983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96226235-T-C

48562455-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96225689-T-A

48562480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96225659-A-G

http://identifiers.org/hco/17/GRCh38#48562513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#96225627-C-A

48563129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96225049-C-T

48563197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96224984-A-G

48563433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96224738-C-T

48563568-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96224602-A-T

48564042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96224183-T-C

48564042-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96224183-T-G

http://identifiers.org/hco/17/GRCh38#48564049-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#96224176-A-C

48564049-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96224176-A-T

48564097-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96224130-T-A

48564097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96224130-T-C

48564217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96224028-T-C

48564327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96223921-C-T

48564399-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96223852-G-T

48564461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96223802-T-C

48564461-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96223802-T-G

48564556-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96223720-C-G

48564556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96223720-C-T

http://identifiers.org/hco/17/GRCh38#48565135-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#96223190-C-A

48565325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96223006-A-G

48565464-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96222863-C-G

48565464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96222863-C-T

48565517-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96222828-G-C

48565517-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96222828-G-T

48565657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96222671-C-T

48565851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96222498-T-C

48565944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96222396-C-T

48566467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96221801-A-G

48566505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96221779-C-T

48566599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96221696-G-A

48566599-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96221696-G-T

48566884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96221387-A-G

48567315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96221050-C-T

48567435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96220930-G-T

48567550-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96220820-C-G

48567604-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96220789-T-G

48567785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96220613-C-T

http://identifiers.org/hco/17/GRCh38#48567951-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#96220275-C-A

48568223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96220003-A-G

48568549-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96219681-C-G

48569067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96219159-T-C

48569989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96218251-T-C

48570083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96218165-A-G

48570489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96217762-G-T

48570919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96217331-C-T

48571161-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96217029-G-C

48571352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96216848-G-A

48571398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96216802-C-T

48571550-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96216584-C-G

48572078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96216062-A-G

48572300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96215857-G-A

48572426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96215744-C-T

http://identifiers.org/hco/17/GRCh38#48572449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#96215727-C-A

48572449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96215727-C-T

48572597-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96215584-G-C

48572601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96215580-A-G

48573138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96214971-C-T

48573331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96214783-G-A

http://identifiers.org/hco/17/GRCh38#48573698-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#96214423-C-A

48573698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96214423-C-T

http://identifiers.org/hco/17/GRCh38#48573738-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#96214379-A-C

http://identifiers.org/hco/17/GRCh38#48574301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#96213759-C-A

48574301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96213759-C-T

http://identifiers.org/hco/17/GRCh38#48574324-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#96213741-C-A

48574324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96213741-C-T

http://identifiers.org/hco/17/GRCh38#48574360-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#96213677-C-A

48574360-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96213677-C-G

48574360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96213677-C-T

http://identifiers.org/hco/17/GRCh38#48574381-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#96213656-A-C

http://identifiers.org/hco/17/GRCh38#48574422-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#96213624-C-A

48574445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96213602-C-T

48574541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96213507-A-G

48575365-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96212648-G-T

http://identifiers.org/hco/17/GRCh38#48575441-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#96212534-C-A

48575461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96212509-G-A

48575782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96212169-T-C

48575955-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96211995-C-G

http://identifiers.org/hco/17/GRCh38#48576064-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#96211888-C-A

48576064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96211888-C-T

48576266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96211668-T-C

48576266-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96211668-T-G

http://identifiers.org/hco/17/GRCh38#48576301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#96211624-C-A

48576459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96211416-T-C

48576459-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96211416-T-G

http://identifiers.org/hco/17/GRCh38#48576467-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#96211408-C-A

48576467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96211408-C-T

48576504-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96211368-G-C

48576504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96211368-G-T

48576566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96211306-C-T

http://identifiers.org/hco/17/GRCh38#48576603-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#96211267-A-C

48576603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96211267-A-G

48576603-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96211267-A-T

48576673-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96211200-T-A

48576673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96211200-T-C

48576673-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96211200-T-G

48577030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96210844-C-T

http://identifiers.org/hco/17/GRCh38#48577792-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#96210117-C-A

48577792-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96210117-C-G

48577792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96210117-C-T

48577937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96209973-T-C

48577937-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96209973-T-G

48577964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96209946-G-A

48577964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96209946-G-T

48577997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96209913-T-C

48578036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96209874-G-A

48578036-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96209874-G-T

48578060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96209850-G-A

48578088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96209825-G-A

48578088-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96209825-G-T

http://identifiers.org/hco/17/GRCh38#48578549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#96209368-C-A

48578549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96209368-C-T

48578643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96209276-G-A

48578643-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96209276-G-C

48578725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96209189-G-A

48578725-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96209189-G-C

48578725-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96209189-G-T

http://identifiers.org/hco/17/GRCh38#48578727-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#96209187-C-A

48579025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96208883-G-A

48579211-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96208701-G-T

48579277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96208634-A-G

48579294-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 96208617-C-G

48579363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96208543-G-A

48579371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96208534-A-G

http://identifiers.org/hco/17/GRCh38#48579470-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#96208424-C-A

48579470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96208424-C-T

http://identifiers.org/hco/17/GRCh38#48579667-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#96208235-C-A

48579667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96208235-C-T

48580259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96207670-A-G

48580529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96207414-A-G

48580556-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96207387-T-C

48580556-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96207387-T-G

48580557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96207386-G-A

48580557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96207386-G-T

48580826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96207102-G-A

48580826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96207102-G-T

48580888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96207040-C-T

48580893-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96207035-G-T

http://identifiers.org/hco/17/GRCh38#48581010-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#96206920-C-A

48581017-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96206913-C-G

48581308-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96206619-A-T

48581516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96206474-T-C

http://identifiers.org/hco/17/GRCh38#48581713-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#96206315-C-A

48581720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96206308-G-A

48581720-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96206308-G-T

http://identifiers.org/hco/17/GRCh38#48581759-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#96206271-C-A

48581791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96206240-T-C

http://identifiers.org/hco/17/GRCh38#48581827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#96206204-C-A

48581899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96206119-A-G

48582030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96205987-G-A

48582030-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96205987-G-C

48582030-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96205987-G-T

48582051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96205966-G-A

48582051-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96205966-G-C

48582051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96205966-G-T

http://identifiers.org/hco/17/GRCh38#48582100-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#96205912-C-A

48582100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96205912-C-T

48582124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96205887-T-C

48582154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 96205852-G-A

48582154-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 96205852-G-T

http://identifiers.org/hco/17/GRCh38#48582225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#96205780-C-A

48582245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 96205764-C-T

48582267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96205742-A-G

http://identifiers.org/hco/17/GRCh38#48582310-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#96205705-C-A

48582310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96205705-C-T

48582414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96205602-C-T

48582709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96205301-A-G

http://identifiers.org/hco/17/GRCh38#48582717-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#96205293-C-A

48582717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96205293-C-T

48583039-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96204949-A-T

48583079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96204922-A-G

http://identifiers.org/hco/17/GRCh38#48583447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#96204649-C-A

48583447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96204649-C-T

48583474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96204622-A-G

48583749-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96204350-G-C

48583750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96204349-C-T

48584022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96204067-A-G

48584355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96203743-T-C

http://identifiers.org/hco/17/GRCh38#48584727-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#96203378-A-C

48584924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96203179-C-T

48585588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 96202526-C-T

48585608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 96202506-C-T

48585795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 96202323-A-G

48585922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96202192-G-A

48585979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96202140-C-T

http://identifiers.org/hco/17/GRCh38#48585983-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#96202136-A-C

48586419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96201690-C-T

48586523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 96201585-C-T

48586879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96201236-G-A

48586950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96201161-C-T

48586959-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96201152-C-G

48587076-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96201077-G-C

48587131-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96201024-G-C

http://identifiers.org/hco/17/GRCh38#48587323-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#96200824-C-A

48587573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96200534-A-G

48587993-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96200170-G-T

48588081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96200085-G-A

48588099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96200048-G-A

48588144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96199979-C-T

http://identifiers.org/hco/17/GRCh38#48588431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#96199691-C-A

48588822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96199282-G-A

48588858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96199218-G-A

48588955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96199125-A-G

48588958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96199122-G-A

48589519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96198599-G-A

http://identifiers.org/hco/17/GRCh38#48589790-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#96198348-C-A

48590000-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96198147-G-T

48590475-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96197677-G-T

48590532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96197621-G-A

48590532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96197621-G-T

http://identifiers.org/hco/17/GRCh38#48590538-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#96197615-C-A

48590688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96197461-G-T

48590846-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96197312-G-T

48590985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96197167-C-T

48591129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96197065-G-T

48591134-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96197060-G-C

48591393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96196811-A-G

http://identifiers.org/hco/17/GRCh38#48591770-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#96196415-C-A

http://identifiers.org/hco/17/GRCh38#48591847-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#96196338-A-C

48591847-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96196338-A-T

48591996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96196181-A-G

48591996-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96196181-A-T

http://identifiers.org/hco/17/GRCh38#48591999-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#96196178-A-C

48591999-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96196178-A-T

http://identifiers.org/hco/17/GRCh38#48592478-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#96195692-C-A

48592494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96195676-T-C

48592494-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96195676-T-G

http://identifiers.org/hco/17/GRCh38#48592597-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#96195573-C-A

48592597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96195573-C-T

48592991-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96195162-T-A

http://identifiers.org/hco/17/GRCh38#48593014-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#96195097-A-C

http://identifiers.org/hco/17/GRCh38#48593091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#96195029-C-A

48593091-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96195029-C-G

48593091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96195029-C-T

48593183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96194937-G-A

48593183-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96194937-G-C

48593213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96194907-G-A

48593213-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96194907-G-C

48593435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96194685-G-A

48593980-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96194141-G-T

48594111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96194011-G-A

48594147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96193985-A-G

48594463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96193675-G-A

48594499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96193637-C-T

48594570-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96193567-G-C

48595614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96192527-T-C

48595639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96192492-G-A

48595775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96192368-G-A

48595775-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96192368-G-C

48595953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96192199-C-T

48596234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96191929-G-A

48596234-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96191929-G-C

48596234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96191929-G-T

48596354-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96191812-G-T

48596375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96191790-G-A

48596375-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96191790-G-T

48596879-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96191278-G-C

48596912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96191246-A-G

http://identifiers.org/hco/17/GRCh38#48597148-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#96191022-A-C

48597148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96191022-A-G

48597161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96191008-T-C

48597161-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96191008-T-G

http://identifiers.org/hco/17/GRCh38#48597186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#96190981-C-A

48597186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96190981-C-T

48597212-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96190956-T-A

48597212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96190956-T-C

48597212-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96190956-T-G

http://identifiers.org/hco/17/GRCh38#48597590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#96190570-C-A

48597590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96190570-C-T

http://identifiers.org/hco/17/GRCh38#48597719-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#96190432-C-A

48597719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96190432-C-T

48597777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96190374-G-A

48597828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96190323-C-T

http://identifiers.org/hco/17/GRCh38#48598167-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#96189984-C-A

48598167-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96189984-C-G

48598167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96189984-C-T

48598422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96189729-C-T

48598642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96189477-T-C

http://identifiers.org/hco/17/GRCh38#48598737-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#96189368-C-A

48598738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96189367-G-A

48598896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96189185-G-A

48598896-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96189185-G-C

48599010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96189067-C-T

48599013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96189064-C-T

48599535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96188597-C-T

48599956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96188202-G-A

48600487-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96187713-G-C

48600698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96187501-T-C

48600949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96187266-G-A

48600984-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96187230-A-T

48601249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96187025-G-A

48601358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96186914-G-A

48601358-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96186914-G-T

48601382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96186888-A-G

48601387-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96186883-G-T

48601414-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96186856-T-A

http://identifiers.org/hco/17/GRCh38#48601483-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#96186807-C-A

48601494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96186790-G-T

http://identifiers.org/hco/17/GRCh38#48601622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#96186653-C-A

48601622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96186653-C-T

48601775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96186504-C-T

http://identifiers.org/hco/17/GRCh38#48601947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#96186327-C-A

48602037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96186220-C-T

48602286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96185968-G-A

48602394-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96185860-G-C

48602426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96185837-C-T

http://identifiers.org/hco/17/GRCh38#48602653-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#96185624-C-A

48602653-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96185624-C-G

http://identifiers.org/hco/17/GRCh38#48602672-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#96185616-C-A

48602672-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96185616-C-G

48603096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96185196-C-T

48603615-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96184673-A-T

48603627-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96184671-T-A

48603627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96184671-T-C

http://identifiers.org/hco/17/GRCh38#48603780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#96184520-C-A

http://identifiers.org/hco/17/GRCh38#48604210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#96184101-C-A

48604280-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96184034-C-G

48604280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96184034-C-T

48604288-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96184026-G-C

http://identifiers.org/hco/17/GRCh38#48604326-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#96183988-A-C

http://identifiers.org/hco/17/GRCh38#48604349-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#96183965-C-A

http://identifiers.org/hco/17/GRCh38#48604378-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#96183936-C-A

48604378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96183936-C-T

http://identifiers.org/hco/17/GRCh38#48604431-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#96183881-A-C

48604546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 96183769-T-C

48604548-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 96183767-T-C

48605423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96182873-T-C

http://identifiers.org/hco/17/GRCh38#48606151-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#96182075-C-A

48606151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: non coding transcript exon variant
orthologous variants: 96182075-C-T

http://identifiers.org/hco/17/GRCh38#48606152-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#96182074-C-A

48606152-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: non coding transcript exon variant
orthologous variants: 96182074-C-G

48606152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: non coding transcript exon variant
orthologous variants: 96182074-C-T

48606176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: non coding transcript exon variant
orthologous variants: 96182055-G-T

48606196-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: non coding transcript exon variant
orthologous variants: 96182035-C-G

48606196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: non coding transcript exon variant
orthologous variants: 96182035-C-T

48606226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: non coding transcript exon variant
orthologous variants: 96182006-G-A

48606226-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: non coding transcript exon variant
orthologous variants: 96182006-G-T

http://identifiers.org/hco/17/GRCh38#48606256-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#96181985-C-A

48606257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: non coding transcript exon variant
orthologous variants: 96181984-T-C

48606257-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: non coding transcript exon variant
orthologous variants: 96181984-T-G

48606278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40283
most severe consequence: non coding transcript exon variant
orthologous variants: 96181974-T-C