75247152-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21904441-T-A

75247723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21905002-A-G

75247829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21905104-G-A

75247829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21905104-G-T

75247871-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21905143-A-T

75247896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21905159-C-T

75247898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21905161-C-T

http://identifiers.org/hco/10/GRCh38#75248109-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#21905355-A-C

75248109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21905355-A-G

75248142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21905388-G-A

75248272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21905515-C-T

http://identifiers.org/hco/10/GRCh38#75248276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#21905519-C-A

75248276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21905519-C-T

75248426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21905648-C-T

75248498-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21905719-C-G

75248564-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21905782-G-T

75248617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21905814-C-T

75249003-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21906020-T-G

75249092-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21906100-C-G

75249160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21906157-G-A

75252660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21908140-G-A

http://identifiers.org/hco/10/GRCh38#75252705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#21908182-C-A

75252833-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21908295-T-A

75252849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21908312-C-T

75252963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21908420-G-A

75253366-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21908801-G-T

http://identifiers.org/hco/10/GRCh38#75253422-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#21908847-C-A

75253436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21908861-A-G

75253573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21909000-A-G

75253758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21909348-G-A

75259865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21913756-C-T

75259879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21913758-A-G

75261343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21915823-G-A

75261791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21916168-T-C

http://identifiers.org/hco/10/GRCh38#75261803-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#21916180-A-C

75261948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21916309-G-A

http://identifiers.org/hco/10/GRCh38#75261959-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#21916320-A-C

75261991-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21916351-A-T

75261996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21916356-G-A

75261996-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21916356-G-C

75262092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21916450-C-T

75262093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21916451-G-A

75262093-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21916451-G-C

75262340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21916701-G-A

75262511-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21916873-T-A

75262511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21916873-T-C

http://identifiers.org/hco/10/GRCh38#75262652-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#21917014-A-C

75262828-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21917207-G-C

75262863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21917242-C-T

75263210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21917560-A-G

75265233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21918334-T-C

75265430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21918595-C-T

75265465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21918648-G-T

75265499-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21918698-T-G

75265804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21918991-G-A

75265833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21919001-T-C

75265881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21919052-G-A

75265884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21919055-G-A

75265884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21919055-G-T

75266221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21919411-T-C

75266221-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21919411-T-G

75266331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21919482-G-A

75278765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21937891-G-A

75278820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21937941-C-T

75278942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21938113-A-G

75279340-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21938472-G-T

http://identifiers.org/hco/10/GRCh38#75279577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#21938668-C-A

75279577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21938668-C-T

75279629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21938718-T-C

75279629-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21938718-T-G

http://identifiers.org/hco/10/GRCh38#75279635-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#21938724-A-C

75279635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21938724-A-G

http://identifiers.org/hco/10/GRCh38#75279656-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#21938742-C-A

75279678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21938768-A-G

75280519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21939911-T-C

75280559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21939932-T-C

75280642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21940009-G-A

75280783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21940168-G-A

75280970-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21940333-G-T

75281124-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21940459-G-T

75282982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21941205-C-T

http://identifiers.org/hco/10/GRCh38#75283130-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#21941363-C-A

75283152-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21941382-G-T

75283160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21941390-A-G

75283200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 21941420-G-A

75283391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 21941609-A-G

75283471-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21941688-G-T

75283494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 21941711-G-T

http://identifiers.org/hco/10/GRCh38#75283520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#21941742-C-A

75283531-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21941756-G-T

http://identifiers.org/hco/10/GRCh38#75283764-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#21941969-A-C

75283764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21941969-A-G

75283850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21942054-C-T

http://identifiers.org/hco/10/GRCh38#75284200-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#21942414-C-A

75284697-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21943018-G-C

75286648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21944058-C-T

http://identifiers.org/hco/10/GRCh38#75286687-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#21944097-C-A

75286952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21944318-C-T

75287070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21944425-T-C

75287304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21944640-C-T

75287405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21944740-A-G

75287760-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21945025-A-T

75287836-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21945094-G-C

75287843-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21945101-A-T

75287866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21945125-G-A

75287866-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21945125-G-T

75288312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21946458-G-A

75288415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21946542-T-C

http://identifiers.org/hco/10/GRCh38#75288417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#21946544-C-A

75288417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21946544-C-T

http://identifiers.org/hco/10/GRCh38#75288426-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#21946553-C-A

75288426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21946553-C-T

75288430-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21946557-G-T

75288544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21946642-T-C

75288561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21946660-G-A

75288561-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21946660-G-T

http://identifiers.org/hco/10/GRCh38#75288591-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#21946665-C-A

75288591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21946665-C-T

75288699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21946691-A-G

75288786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21946770-G-A

http://identifiers.org/hco/10/GRCh38#75288952-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#21946939-C-A

75289174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21947151-T-C

75289344-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21947268-C-G

75291812-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21950476-T-A

75291812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21950476-T-C

75291896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21951124-G-A

75291989-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21951200-T-A

http://identifiers.org/hco/10/GRCh38#75291999-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#21951210-C-A

75292072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21951280-T-C

75292169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21951361-G-A

75293030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21952416-C-T

75293297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21952702-G-A

75293335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21952740-C-T

http://identifiers.org/hco/10/GRCh38#75293455-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#21952829-C-A

http://identifiers.org/hco/10/GRCh38#75293834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#21953081-C-A

75293834-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21953081-C-G

75294168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 21953348-C-T

75294331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21953507-C-T

75294343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21953519-G-A

75294473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21953600-A-G

http://identifiers.org/hco/10/GRCh38#75294656-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#21953781-C-A

75294656-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 21953781-C-G

http://identifiers.org/hco/10/GRCh38#75295053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#21954116-C-A

75295053-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21954116-C-G

75295053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21954116-C-T

75295117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 21954177-G-A

75295301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 21954355-G-A

http://identifiers.org/hco/10/GRCh38#75296221-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#21955270-C-A

http://identifiers.org/hco/10/GRCh38#75296284-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#21955331-C-A

75296284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21955331-C-T

75296285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21955332-A-G

75296355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21955395-T-C

75296454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21955434-G-A

75296611-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21955585-G-C

75296611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21955585-G-T

75296640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21955616-G-A

75297104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21955845-C-T

75297117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21955858-T-C

http://identifiers.org/hco/10/GRCh38#75303008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#21967197-C-A

75303085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21967273-T-C

75303205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21967387-C-T

75304490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21968419-C-T

75305210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21969308-A-G

75337922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21981830-G-A

75338316-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21982151-C-G

75338525-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21982351-T-G

http://identifiers.org/hco/10/GRCh38#75338560-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#21982387-C-A

http://identifiers.org/hco/10/GRCh38#75338801-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#21982608-A-C

75338918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21982697-C-T

75339462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21983676-A-G

75339792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21984000-A-G

75340497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21984375-C-T

75340566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21984441-T-C

75341652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21986077-G-A

http://identifiers.org/hco/10/GRCh38#75342106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#21986527-C-A

75342310-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21986732-G-C

75342311-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21986733-G-T

75342439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21986869-C-T

75342460-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21986890-G-T

http://identifiers.org/hco/10/GRCh38#75343089-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#21989024-A-C

75343089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21989024-A-G

75343089-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21989024-A-T

75343354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21989277-G-A

75343354-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21989277-G-T

75343410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21989337-T-C

75343898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21989812-C-T

75343919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21989831-C-T

75344270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21990175-G-A

75344425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21990328-C-T

75344526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21990420-C-T

75344606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21990470-A-G

75345151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21991141-C-T

75345359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21991359-C-T

http://identifiers.org/hco/10/GRCh38#75347031-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#21992543-C-A

75347079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21992627-C-T

75347112-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21992660-T-G

75347126-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21992667-T-G

http://identifiers.org/hco/10/GRCh38#75347157-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#21992680-A-C

75347157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21992680-A-G

75347250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21992770-C-T

75347286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21992806-C-T

75347299-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21992818-T-A

75347299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21992818-T-C

75347300-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21992819-G-C

75347566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21992974-T-C

75349509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21994631-G-A

75349756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21995077-C-T

75350155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21995478-C-T

75350262-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21995582-A-T

75350949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21996575-G-A

75351638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21996930-A-G

75351753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21997034-T-C

75351974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21997232-C-T

75352019-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21997277-C-G

75352062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21997320-C-T

75352522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21997720-C-T

75352523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21997721-G-A

http://identifiers.org/hco/10/GRCh38#75352618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#21997829-C-A

75352618-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21997829-C-G

http://identifiers.org/hco/10/GRCh38#75352720-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#21998058-A-C

75353071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21998542-G-A

75353378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21998850-G-A

75355692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21999706-T-C

http://identifiers.org/hco/10/GRCh38#75355996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#21999969-C-A

75356176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22000169-G-A

75357876-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22001666-C-G

http://identifiers.org/hco/10/GRCh38#75357977-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#22001753-C-A

75357981-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22001757-C-G

75357981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22001757-C-T

75357989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22001765-A-G

75358009-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22001799-T-C

75358177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22001931-A-G

75358652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22002419-C-T

75358656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22002423-G-A

http://identifiers.org/hco/10/GRCh38#75358694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#22002461-C-A

75358694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22002461-C-T

http://identifiers.org/hco/10/GRCh38#75358733-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#22002500-C-A

75358733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22002500-C-T

75358783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22002560-G-T

75358968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22002742-G-A

75359376-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22003138-G-T

75359562-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22003385-C-G

http://identifiers.org/hco/10/GRCh38#75359717-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#22003532-C-A

75360493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22005474-A-G

75360567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22005548-G-A

75360567-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22005548-G-T

75360597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22005578-G-T

75360676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22005649-C-T

75360756-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22005725-C-G

75360756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22005725-C-T

http://identifiers.org/hco/10/GRCh38#75360813-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#22006253-A-C

http://identifiers.org/hco/10/GRCh38#75360819-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#22006259-C-A

75360819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22006259-C-T

75360912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22006346-T-C

75360950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22006381-G-A

75360957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22006388-G-A

75360957-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22006388-G-T

http://identifiers.org/hco/10/GRCh38#75360979-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#22006410-C-A

75361032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22006461-A-G

http://identifiers.org/hco/10/GRCh38#75361034-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#22006463-C-A

75361034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22006463-C-T

75361365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22006726-G-A

75361365-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22006726-G-T

75361448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22006801-A-G

75361455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22006808-T-C

75361466-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22006819-G-T

75361482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22006835-G-A

75361482-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22006835-G-C

75361482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22006835-G-T

75361497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22006850-T-C

75361498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22006851-G-A

75361695-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22007030-T-A

75361695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22007030-T-C

75361713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22007583-T-C

75361718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22007588-C-T

http://identifiers.org/hco/10/GRCh38#75361763-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#22007637-C-A

http://identifiers.org/hco/10/GRCh38#75361766-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#22007640-C-A

75361766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22007640-C-T

75361993-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22007860-A-T

75362118-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22007976-C-G

75362540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22008381-C-T

75362684-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22008525-A-T

75362771-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22008612-G-T

75362812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22008659-G-A

75362812-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22008659-G-C

75362812-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22008659-G-T

75362819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22008682-C-T

http://identifiers.org/hco/10/GRCh38#75362947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#22008802-C-A

75362947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22008802-C-T

75363040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22008920-G-A

http://identifiers.org/hco/10/GRCh38#75363220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#22009136-C-A

75363322-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22009238-T-G

http://identifiers.org/hco/10/GRCh38#75363344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#22009261-C-A

75363663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22009471-G-A

75363782-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22009592-A-T

75363951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22009765-G-A

75364207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22010030-T-C

75364207-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22010030-T-G

75364210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22010033-G-A

75364258-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22010097-G-T

http://identifiers.org/hco/10/GRCh38#75364656-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#22011219-C-A

75365171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22011926-C-T

75367288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22012902-T-C

75367876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22013461-A-G

75367883-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22013468-G-C

75367999-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22013572-A-T