207761029-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 194765322-A-T

207761140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 194765211-A-G

207761162-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 194765191-A-T

207761178-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 194765175-A-T

http://identifiers.org/hco/1/GRCh38#207761528-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#194764838-A-C

207761528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 194764838-A-G

207761562-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 194764804-G-T

207761647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 194764732-T-C

http://identifiers.org/hco/1/GRCh38#207761916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#194764441-C-A

207761954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 194764408-T-C

207762345-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 194763891-T-A

207766991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 194760162-T-C

207767026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 194760129-A-G

207767251-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 194759902-T-G

http://identifiers.org/hco/1/GRCh38#207767477-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#194759508-A-C

207767477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 194759508-A-G

207767482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 194759503-A-G

207767549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 194759437-T-C

207767549-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 194759437-T-G

207767710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 194759303-T-C

207767710-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 194759303-T-G

http://identifiers.org/hco/1/GRCh38#207767785-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#194759229-C-A

207767835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 194759183-T-C

207767916-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 194759107-T-G

207768037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 194758973-A-G

207770095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 194758088-A-G

207770175-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 194758017-G-C

207770175-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 194758017-G-T

http://identifiers.org/hco/1/GRCh38#207770304-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#194757879-C-A

207770304-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 194757879-C-G

207770304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 194757879-C-T

207777327-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 194757356-A-T

207783302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 194750464-A-G

http://identifiers.org/hco/1/GRCh38#207783556-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#194750148-C-A

207783556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 194750148-C-T

http://identifiers.org/hco/1/GRCh38#207783649-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#194750056-C-A

207783649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 194750056-C-T

http://identifiers.org/hco/1/GRCh38#207783695-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#194750009-C-A

207783695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 194750009-C-T

207785131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 194746970-A-G

207785131-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 194746970-A-T

207785165-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 194746942-T-G

207785233-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 194746860-C-G

http://identifiers.org/hco/1/GRCh38#207785237-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#194746856-A-C

207785237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 194746856-A-G

207785584-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 194744753-G-C

http://identifiers.org/hco/1/GRCh38#207785820-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#194744567-C-A

207785861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 194744528-A-G

207785982-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 194744408-G-T

207786206-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 194744216-A-T

207786210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 194744212-G-T

207786212-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 194744210-G-T

207786752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 194729592-A-G

207787635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 194729069-T-C

207787696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 194729003-C-T

207788916-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 194726676-C-G

207789300-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 194726196-T-C

207789495-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 194725976-A-T

207789731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 194725747-C-T

207789865-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 194725561-G-T

http://identifiers.org/hco/1/GRCh38#207789867-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#194725559-C-A

207789867-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 194725559-C-G

207789867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 194725559-C-T

207794813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 194725006-T-C

207794834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 194724987-A-G

207794838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 194724983-T-C

207795014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 194724814-A-G

207795629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194724111-A-G

207796069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194723710-C-T

207796076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194723703-G-A

207797037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194723303-T-C

207798372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194722538-C-T

207798375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194722535-C-T

207798432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194722477-G-A

207799482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194721703-A-G

207799763-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194721557-A-T

207799831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194721485-T-C

207800036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194721299-A-G

207800104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194721228-T-C

207800182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194721156-T-C

http://identifiers.org/hco/1/GRCh38#207800303-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#194721037-A-C

http://identifiers.org/hco/1/GRCh38#207801477-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#194720254-C-A

207801477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194720254-C-T

207801501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194720230-G-A

http://identifiers.org/hco/1/GRCh38#207801780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#194720004-C-A

207801780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 194720004-C-T

http://identifiers.org/hco/1/GRCh38#207801943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#194719849-C-A

207801943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 194719849-C-T

http://identifiers.org/hco/1/GRCh38#207802027-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#194719761-C-A

http://identifiers.org/hco/1/GRCh38#207802172-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#194719655-C-A

207802172-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 194719655-C-G

207802252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 194719593-T-C

207802252-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 194719593-T-G

207802292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 194719556-T-C

207802320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 194719529-G-A

207802320-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 194719529-G-C

207802389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 194719480-T-C

207802419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 194719450-C-T

207802876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194719082-G-A

207802876-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194719082-G-C

207802876-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194719082-G-T

207802931-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194719037-G-C

http://identifiers.org/hco/1/GRCh38#207803297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#194718746-C-A

207803335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194718702-G-A

207803657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194718425-T-C

207803738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194718362-A-G

207803738-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194718362-A-T

207803772-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194718328-G-T

207804008-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194718071-T-A

207804019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194718054-T-C

207804123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194717934-T-C

http://identifiers.org/hco/1/GRCh38#207804192-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#194717862-C-A

http://identifiers.org/hco/1/GRCh38#207804258-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#194717797-C-A

207804258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194717797-C-T

http://identifiers.org/hco/1/GRCh38#207804317-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#194717770-A-C

207804317-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194717770-A-T

207804481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 194717665-G-T

207804503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 194717640-G-A

207804503-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 194717640-G-T

207804633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 194717559-T-C

207804694-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194717508-G-T

207804777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194717450-C-T

207804814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194717419-G-T

http://identifiers.org/hco/1/GRCh38#207804815-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#194717418-C-A

207804815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194717418-C-T

207805048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194717192-A-G

207805150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194717101-A-G

207805409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 194716853-G-A

207805409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 194716853-G-T

207805454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194716810-G-A

207805454-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194716810-G-T

207805691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194716734-A-G

207806231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194716229-C-T

http://identifiers.org/hco/1/GRCh38#207806235-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#194716225-C-A

207806287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194716134-G-A

207806287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194716134-G-T

207806333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194716089-G-A

207806333-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194716089-G-T

207806369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194716060-G-A

207806369-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194716060-G-T

207806512-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194715998-T-A

207806512-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194715998-T-C

http://identifiers.org/hco/1/GRCh38#207806514-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#194715996-C-A

207806514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194715996-C-T

207806553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194715957-C-T

207806572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194715938-G-A

207806572-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194715938-G-T

207806574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194715921-A-G

http://identifiers.org/hco/1/GRCh38#207806601-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#194715895-C-A

207806601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194715895-C-T

207806727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194715733-G-A

207806727-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194715733-G-T

http://identifiers.org/hco/1/GRCh38#207806770-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#194715696-C-A

207806935-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 194715556-G-T

207806971-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194715520-G-T

http://identifiers.org/hco/1/GRCh38#207806987-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#194715514-C-A

207806987-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194715514-C-G

207807081-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194715443-G-C

207807095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194715429-G-A

207807095-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194715429-G-T

207807320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 194715217-T-C

207807411-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194715139-G-C

207807520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194715058-C-T

207807767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194714818-G-A

207807767-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194714818-G-C

207807770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194714815-G-A

207807770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194714815-G-T

207807894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194714706-A-G

207807925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194714674-G-A

207807925-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194714674-G-T

http://identifiers.org/hco/1/GRCh38#207808026-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#194714585-C-A

207808026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194714585-C-T

207808048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194714565-G-A

207808271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194714331-A-G

207808443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194714163-G-A

207808443-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194714163-G-T

http://identifiers.org/hco/1/GRCh38#207808486-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#194714074-A-C

207808940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194713441-G-A

http://identifiers.org/hco/1/GRCh38#207809093-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#194713303-C-A

207809093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194713303-C-T

207809284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194713068-G-T

207809289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194713063-G-A

207809289-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194713063-G-T

http://identifiers.org/hco/1/GRCh38#207809308-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#194713044-C-A

207809385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194713007-T-C

207809456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194712948-G-A

http://identifiers.org/hco/1/GRCh38#207809593-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#194712835-C-A

207809593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194712835-C-T

207809664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194712766-G-T

207810047-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194711857-A-T

207810251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 194711657-G-A

207810683-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194711316-G-C

207810683-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194711316-G-T

207811027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 194711122-T-C

207811040-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194711109-C-G

207811601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194710837-C-T

207811650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194710795-A-G

207811857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194710553-C-T

http://identifiers.org/hco/1/GRCh38#207812153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#194710321-C-A

207812171-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 194710303-G-T

http://identifiers.org/hco/1/GRCh38#207812211-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#194710272-C-A

207812211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 194710272-C-T

207812256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 194710225-G-A

207812256-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 194710225-G-T

207812266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 194710214-G-A

207812266-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 194710214-G-C

207812516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194709996-G-A

207812516-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194709996-G-T

207812582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194709945-T-C

207812614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194709914-T-C

207812692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194709839-C-T

207812897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194709529-G-A

http://identifiers.org/hco/1/GRCh38#207813033-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#194709437-C-A

207813170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194709326-T-C

207813197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194709299-A-G

http://identifiers.org/hco/1/GRCh38#207813424-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#194709101-C-A

207813424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194709101-C-T

http://identifiers.org/hco/1/GRCh38#207813495-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#194709040-C-A

207813766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 194708842-A-G

207813972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 194708652-G-A

207813972-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 194708652-G-T

207813980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 194708642-G-A

207813980-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 194708642-G-T

207814017-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 194708605-T-A

207814017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 194708605-T-C

http://identifiers.org/hco/1/GRCh38#207814066-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#194708556-C-A

207814209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 194708472-A-G

207814231-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 194708450-G-T

207814248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 194708433-C-T

http://identifiers.org/hco/1/GRCh38#207814282-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#194708399-C-A

207814424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 194708354-A-G

207814659-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 194708288-G-T

207814900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 194708049-T-C

207814905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 194708044-T-C

207814920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 194708029-G-A

207814920-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 194708029-G-T

http://identifiers.org/hco/1/GRCh38#207815276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#194707719-C-A

http://identifiers.org/hco/1/GRCh38#207815395-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#194707637-C-A

207815444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 194707603-A-G

http://identifiers.org/hco/1/GRCh38#207815452-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#194707595-C-A

207815513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 194707538-G-A

207815513-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 194707538-G-T

207815651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 194707420-G-A

207815651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 194707420-G-T

207815840-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 194707253-G-T

207816308-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194706850-G-C

http://identifiers.org/hco/1/GRCh38#207816311-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#194706847-A-C

207816311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194706847-A-G

207816312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194706846-G-A

207816354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194706804-A-G

207816596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194706569-C-T

http://identifiers.org/hco/1/GRCh38#207817146-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#194706111-A-C

207817146-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194706111-A-T

207817164-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194706096-G-T

http://identifiers.org/hco/1/GRCh38#207817377-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#194705893-C-A

207817377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: non coding transcript exon variant
orthologous variants: 194705893-C-T

http://identifiers.org/hco/1/GRCh38#207817453-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#194705816-C-A

207817733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194705588-A-G

207817736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194705585-C-T

207817746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194705575-G-A

207818596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 194704873-G-A

207818739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 194704741-C-T

http://identifiers.org/hco/1/GRCh38#207818844-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#194704647-C-A

http://identifiers.org/hco/1/GRCh38#207818923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#194704516-C-A

207818923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 194704516-C-T

http://identifiers.org/hco/1/GRCh38#207819032-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#194704410-C-A

207819103-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 194704336-T-G

207819244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 194704075-G-A

http://identifiers.org/hco/1/GRCh38#207819267-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#194704053-C-A

207819267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 194704053-C-T

http://identifiers.org/hco/1/GRCh38#207819303-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#194704016-C-A

207819493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 194703848-T-C

207819935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 194703411-A-G

207820091-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 194703315-C-G

207820369-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 194703030-T-A

http://identifiers.org/hco/1/GRCh38#207821124-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#194702238-A-C

207821162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 194702200-C-T

207821284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 194702091-T-C

207821284-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 194702091-T-G

207822013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 194701421-G-A

207822048-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 194701393-G-C

207822154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 194701294-C-T

207822293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 194701159-A-G

207822336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 194701119-G-A

207822570-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 194700883-T-A

207822570-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 194700883-T-G

207822639-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 194700815-G-C

http://identifiers.org/hco/1/GRCh38#207823160-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#194700304-A-C

207823160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 194700304-A-G

207823460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 194700018-C-T

207824666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194698615-A-G

207825055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194698267-T-C

207825135-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194698205-T-A

207825453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 194697919-C-T

207826786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194696891-G-A

207827090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194696612-G-A

http://identifiers.org/hco/1/GRCh38#207827265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#194696444-C-A

207827356-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194696364-C-G

http://identifiers.org/hco/1/GRCh38#207827902-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#194695811-C-A

http://identifiers.org/hco/1/GRCh38#207827916-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#194695799-A-C

http://identifiers.org/hco/1/GRCh38#207827959-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#194695756-C-A

207828069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194695656-G-A

207828217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194695535-T-C

207828495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194695279-G-A

207828598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 194695179-A-G

207828990-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194694840-A-T

207829182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194694664-T-C

http://identifiers.org/hco/1/GRCh38#207830262-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#194693486-A-C

207831245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194693145-A-G

207831359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194693029-T-C

207831441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194692953-C-T

207831702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 194692759-T-C

http://identifiers.org/hco/1/GRCh38#207831998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#194692513-C-A

207832188-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 194692316-G-C

207832733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194690624-G-A

207832928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194690503-C-T

207832937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194690494-C-T

207833571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194690236-C-T

207833896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194689852-T-C

http://identifiers.org/hco/1/GRCh38#207833935-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#194689818-A-C

207834976-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194689244-C-G

http://identifiers.org/hco/1/GRCh38#207835763-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#194688551-C-A

207835763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194688551-C-T

http://identifiers.org/hco/1/GRCh38#207836276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#194688073-C-A

207836276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194688073-C-T

207836889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194687560-A-G

http://identifiers.org/hco/1/GRCh38#207837274-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#194687260-A-C

207837591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194686972-G-A

207837652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194686907-G-A

207837652-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194686907-G-C

207837922-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194686646-G-C

207837935-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194686633-T-A

207837935-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194686633-T-G

207838009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194686562-A-G

207838577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194685997-T-C

207838615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194685960-G-A

207838902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194685687-A-G

207839245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194685439-C-T

207839353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194685316-T-C

207840513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194683895-C-T

207840652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194683767-C-T

207840716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194683604-T-C

207840800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194683495-C-T

http://identifiers.org/hco/1/GRCh38#207841173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#194682943-C-A

207841173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194682943-C-T

http://identifiers.org/hco/1/GRCh38#207841606-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#194682487-C-A

207841924-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194682259-G-T

207842262-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194682007-G-C

207844850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194681462-C-T

207845151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194681167-A-G

207845318-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194681039-G-C

207845369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194680989-G-A

207845433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194680925-C-T

207845472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194680886-G-A

207846210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194679438-T-C

207846285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194679373-C-T

207846442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194679217-T-C

207846906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194678802-T-C

207847853-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194678180-G-C

207848041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194678010-A-G

207849039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194677139-T-C

207849351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194676821-G-A

207849573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194676612-T-C

207850810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194675518-C-T

207850851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194675507-G-A

207850851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194675507-G-T

207852038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194674354-A-G

207852135-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194674257-G-C

207852163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194674240-G-A

207852574-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194673866-G-C

207852716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194673747-A-G

207853259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194673214-A-G

207853620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194672860-A-G

207853646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194672834-T-C

207855265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194671562-T-C

207855279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194671549-C-T

207855401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194671446-G-A

207855452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194671336-T-C

207856053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194670675-C-T

207856081-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194670646-A-T

207856233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194670510-A-G

207858824-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194668124-T-A

207858851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194668097-G-A

207858851-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194668097-G-C

207859051-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194667931-T-A

207859058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194667923-A-G

207859063-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194667918-G-C

207859533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194667509-T-C

207859584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194667466-G-A

207860509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194666905-G-A

http://identifiers.org/hco/1/GRCh38#207860902-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#194666586-A-C

207860966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194666519-A-G

207861079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194666406-T-C

http://identifiers.org/hco/1/GRCh38#207861905-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#194665490-C-A

207861953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194665465-A-G

207862242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194665089-T-C

207862463-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194664868-T-G

207862465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194664866-G-A

207862465-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194664866-G-C

207862529-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194664827-T-A

207862529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194664827-T-C

207862666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194664706-T-C

http://identifiers.org/hco/1/GRCh38#207862897-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#194664496-A-C

207863787-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194663649-T-G

207863870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194663585-C-T

207864176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194663260-G-T

207864938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194662480-C-T

207864977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194662445-T-C

207865404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194662081-T-C

207866357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194661022-G-A

207866809-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194660662-G-T

207866858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194660622-C-T

207867158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194660319-T-C

http://identifiers.org/hco/1/GRCh38#207867822-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#194659715-C-A

http://identifiers.org/hco/1/GRCh38#207868055-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#194659544-A-C

207868062-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194659527-A-T

207868568-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194659083-A-T

207868887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194658845-C-T

207869035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 194658758-G-A

207869035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 194658758-G-T

207869050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 194658744-G-A

207869050-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 194658744-G-C

207869050-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 194658744-G-T

http://identifiers.org/hco/1/GRCh38#207869056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#194658738-C-A

207869056-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 194658738-C-G

207869056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 194658738-C-T

http://identifiers.org/hco/1/GRCh38#207869088-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#194658716-C-A

207869088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 194658716-C-T

http://identifiers.org/hco/1/GRCh38#207869211-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#194658642-C-A

207869363-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 194658543-C-G

207869363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 194658543-C-T

207869522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 194658419-A-G

207869681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194658332-A-G

207869709-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194658310-G-T

http://identifiers.org/hco/1/GRCh38#207869979-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#194658009-A-C

207869979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: non coding transcript exon variant
orthologous variants: 194658009-A-G

207870022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: non coding transcript exon variant
orthologous variants: 194657848-G-A

207870022-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: non coding transcript exon variant
orthologous variants: 194657848-G-T

207870417-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194657332-C-G

207871771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194655304-G-A

207872781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194654089-C-T

207872908-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194653976-T-G

207873003-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194653884-T-G

http://identifiers.org/hco/1/GRCh38#207873572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#194648792-C-A

207873880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 194648494-G-A

207873880-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 194648494-G-T

207874031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 194648356-G-T

207874048-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 194648343-G-T

http://identifiers.org/hco/1/GRCh38#207874889-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#194647684-C-A

207875436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194647284-T-C

207875487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194647260-C-T

207875551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194647241-T-C

207876213-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 194646500-T-G

207876667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194646098-G-T

207876749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 194646018-C-T