37951985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94827382-A-G

37952091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94827486-G-A

http://identifiers.org/hco/21/GRCh38#37952109-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94827504-C-A

37952254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94827648-C-T

37952493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94827890-G-A

37952659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94827973-G-A

http://identifiers.org/hco/21/GRCh38#37952697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94827994-C-A

37952697-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94827994-C-G

37952713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94828009-G-A

37952713-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94828009-G-T

37952731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94828030-G-A

37952731-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94828030-G-T

37952736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94828035-A-G

37952740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94828039-A-G

37952740-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94828039-A-T

37952747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94828046-G-A

37952747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94828046-G-T

http://identifiers.org/hco/21/GRCh38#37952762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94828061-C-A

37952762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94828061-C-T

http://identifiers.org/hco/21/GRCh38#37952789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94828092-C-A

37952789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94828092-C-T

http://identifiers.org/hco/21/GRCh38#37952843-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94828144-C-A

37952851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 94828152-G-A

37952903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 94828196-C-T

37952904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 94828197-T-C

37952907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 94828200-G-A

37952907-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 94828200-G-T

37952933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 94828226-C-T

37952935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 94828228-A-G

37953000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 94828293-T-C

37953089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94828379-G-A

37953089-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94828379-G-T

37953099-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94828389-G-T

http://identifiers.org/hco/21/GRCh38#37953106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94828396-C-A

37953140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94828424-A-G

http://identifiers.org/hco/21/GRCh38#37953312-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94828558-A-C

37953312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94828558-A-G

37953420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94828659-A-G

37953606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94829902-C-T

37953651-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94829947-T-A

37953661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94829967-G-A

37953870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94830163-A-G

37954095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94830388-C-T

http://identifiers.org/hco/21/GRCh38#37954162-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94830416-A-C

37954267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94830521-G-A

37954390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94830634-G-A

37954485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94830732-T-C

37957867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94832323-G-A

37957879-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94832335-G-C

37957914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94832370-A-G

37958094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94832562-T-C

37958315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94833865-G-A

37958322-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94833872-G-C

37958360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94833918-A-G

37958511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94834068-C-T

37958670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94834229-T-C

37958758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94834300-G-A

37958788-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94834330-G-T

37958790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94834332-G-A

37958874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94834414-G-A

37958874-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94834414-G-C

37958998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94834537-C-T

http://identifiers.org/hco/21/GRCh38#37960177-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94835128-C-A

http://identifiers.org/hco/21/GRCh38#37960202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94835151-C-A

37960218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94835167-A-G

37960218-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94835167-A-T

37960266-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94835195-T-A

37960387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94835260-T-C

37960449-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94835306-A-T

37960623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94835477-C-T

37960843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94835646-T-C

http://identifiers.org/hco/21/GRCh38#37961078-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94835884-C-A

37961218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94836021-T-C

37961238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94836046-T-C

http://identifiers.org/hco/21/GRCh38#37961320-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94836120-C-A

37961496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94836252-A-G

37961513-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94836269-G-T

37964846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94840352-A-G

37964985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94840486-G-A

37964985-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94840486-G-C

37965142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94840669-G-A

37965147-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94840670-T-G

37965535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94841055-C-T

37965571-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94841085-G-C

37965851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94841307-G-A

37965853-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94841309-T-A

http://identifiers.org/hco/21/GRCh38#37965874-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94841330-C-A

37965874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94841330-C-T

37965911-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94841367-T-G

37966261-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94841681-G-T

37966583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94842969-C-T

37966600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94842984-C-T

37967133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94843535-T-C

37967198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94843583-G-A

37967306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94843645-G-A

37967405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94843744-T-C

http://identifiers.org/hco/21/GRCh38#37967654-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94844005-A-C

37967898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94844220-T-C

37967997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94844317-C-T

37968164-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94844416-C-G

37968284-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94844511-T-A

37968503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94845168-A-G

37968557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94845213-C-T

37968718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94845364-G-A

37968718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94845364-G-T

37968726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94845372-C-T

37968732-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94845377-A-T

37968947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94845603-T-C

37969121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94845768-G-A

37969330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94845947-G-A

37969803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94847088-T-C

37969827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94847112-G-A

37970123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94847413-C-T

37970175-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94847552-C-G

37970797-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94848201-G-C

37970809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94848214-T-C

http://identifiers.org/hco/21/GRCh38#37970810-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94848215-A-C

37970869-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94848921-G-T

http://identifiers.org/hco/21/GRCh38#37970901-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94848953-A-C

37971172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94849200-C-T

37971203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94849230-C-T

37971328-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94849356-T-G

37971542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94849561-A-G

http://identifiers.org/hco/21/GRCh38#37971989-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94850470-C-A

37972121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94850557-T-C

37972139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94850594-G-A

37972354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94850757-A-G

http://identifiers.org/hco/21/GRCh38#37972575-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94850981-A-C

37972582-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94850988-T-A

37972691-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94851093-G-C

37972691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94851093-G-T

37972865-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94851245-C-G

37972896-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94851276-C-G

37980233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94851661-A-G

37980453-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94851873-G-T

37980476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94851897-T-C

37980617-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94852040-T-G

http://identifiers.org/hco/21/GRCh38#37981133-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94852753-A-C

37981279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94852869-C-T

37986678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94854419-G-A

37986686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94854427-C-T

37986730-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94854464-G-T

37986752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94854486-G-A

37987261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94855478-T-C

37987444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94855614-T-C

37987445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94855615-G-T

37987601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94855691-T-C

37987687-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94855768-G-C

37987880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94855984-G-A

http://identifiers.org/hco/21/GRCh38#37987923-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94856022-A-C

37987923-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94856022-A-T

37988764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94856150-C-T

37988776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94856161-T-C

37988776-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94856161-T-G

37988832-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94856208-A-T

37988880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94856257-G-A

http://identifiers.org/hco/21/GRCh38#37988914-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94856287-A-C

37989049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94856416-G-A

37989144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94856510-T-C

37989198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94856558-G-A

37990144-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94859071-G-C

37990165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94859090-G-A

37990254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94859161-G-A

37990377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94859289-C-T

37990385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94859297-A-G

37990949-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94859833-T-G

37992726-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94862771-G-T

http://identifiers.org/hco/21/GRCh38#37992728-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94862773-C-A

37992744-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94862793-C-G

37992744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94862793-C-T

37993089-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94863123-C-G

37993228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94863244-C-T

37993385-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94863357-G-T

http://identifiers.org/hco/21/GRCh38#37993935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94864174-C-A

37993984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94864227-A-G

37994049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94864291-G-A

37994213-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94864470-G-C

37994251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94864504-C-T

http://identifiers.org/hco/21/GRCh38#37994258-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94864511-A-C

http://identifiers.org/hco/21/GRCh38#37994297-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94864547-A-C

37994604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94865229-T-C

37994613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94865238-A-G

http://identifiers.org/hco/21/GRCh38#37994941-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94865585-A-C

37995135-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94865840-G-C

38002365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94868297-C-T

38002427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94868390-T-C

38002986-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94868880-G-T

38003248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94869103-A-G

38003426-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94869263-T-A

38003484-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94869321-C-G

38003523-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94869397-T-G

38003577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94869451-C-T

38003693-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94869534-A-T

38003861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94869672-T-C

38004103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94869886-G-A

38004167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94869935-C-T

38005722-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94870866-G-T

38005855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94870997-G-A

38005855-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94870997-G-C

38006182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94871279-A-G

38006400-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94871481-T-A

38006426-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94871506-G-T

38006554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94871638-G-T

http://identifiers.org/hco/21/GRCh38#38006636-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94871691-C-A

38006665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94871720-T-C

http://identifiers.org/hco/21/GRCh38#38006683-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94871736-C-A

38006777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94871844-T-C

38006912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94871949-T-C

38006972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94872012-G-A

38006972-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94872012-G-T

38007004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94872044-C-T

38007016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94872058-A-G

38007089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94872109-C-T

38007100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94872120-C-T

38007217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94872242-G-A

38007300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94872321-G-T

38007326-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94872346-G-C

38009228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94875244-C-T

38009318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94875331-T-C

38009399-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94875407-T-G

38009720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94875688-C-T

38009726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94875694-C-T

38009809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94875760-G-A

38009905-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94875842-A-T

38009912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94875851-T-C

38009990-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94875930-T-G

38010283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94876718-C-T

http://identifiers.org/hco/21/GRCh38#38010367-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94876790-C-A

38010446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94876846-A-G

38010920-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94877050-T-A

38011322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94877446-C-T

38011454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94877564-C-T

38014418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94881056-C-T

38014544-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94881165-A-T

38014604-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94881199-G-C

38014605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94881200-C-T

38014727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94881298-C-T

38014806-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94881377-C-G

38014860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94881411-C-T

38014892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94881421-T-C

38014958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94881473-G-A

38015158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94881668-G-A

38015158-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94881668-G-C

http://identifiers.org/hco/21/GRCh38#38015188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94881701-C-A

38015239-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94881769-A-T

38015335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94881879-A-G

38015849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94882384-C-T

38016047-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94882438-G-T

38016140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94882450-A-G

38016343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94882542-A-G

38016568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94890173-C-T

38018911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94890240-A-G

38019031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94890366-G-T

38019234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94890565-G-A

38019478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94891200-A-G

38023130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94893727-C-T

38023152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94893750-T-C

38023300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94893885-C-T

38023400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94893974-C-T

38023414-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94893988-T-A

38023559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94894158-T-C

38023562-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94894161-T-G

http://identifiers.org/hco/21/GRCh38#38027547-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94895749-C-A

38027958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94896135-C-T

38028016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 94896184-T-C

38028027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94896195-T-C

38028880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94897274-A-G

38029075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94897467-A-G

38029195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94897567-T-C

38030013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94898213-C-T

http://identifiers.org/hco/21/GRCh38#38030060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94898256-C-A

38030076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94898272-A-G

38030285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94898459-G-T

38030405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94898552-C-T

38030610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94898730-T-C

38032195-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94900948-G-C

38032411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94901139-A-G

38032915-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94901585-G-T

38033105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94901730-T-C

38033105-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94901730-T-G

38033189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94901811-C-T

38037095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94904375-G-A

http://identifiers.org/hco/21/GRCh38#38037139-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94904401-C-A

38037139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94904401-C-T

38037271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94904524-A-G

38037457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94904690-G-A

38037457-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94904690-G-T

38037577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94904809-G-A

38037858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94905021-C-T

38037901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94905063-T-C

38038117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94905290-C-T

38038135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94905307-C-T

38038187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94905352-C-T

38038328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94905485-A-G

38038410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94905564-C-T

38038686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94905764-T-C

38038711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94905788-A-G

38038746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94905822-G-A

38047854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94919076-A-G

38048077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94918857-T-C

38048374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94918565-G-A

38048420-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94918520-T-G

38048695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94918271-A-G

38048790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94918181-G-A

http://identifiers.org/hco/21/GRCh38#38054284-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94920122-A-C

http://identifiers.org/hco/21/GRCh38#38054538-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94920361-C-A

38054538-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94920361-C-G

38054538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94920361-C-T

38054679-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94920481-C-G

38054709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94920508-C-T

38054715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94920514-G-A

http://identifiers.org/hco/21/GRCh38#38054834-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94920627-A-C

38054863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94920658-T-C

38054913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94920706-G-A

38054987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94920763-G-A

38054994-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94920770-C-G

38054994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94920770-C-T

38055080-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94920806-G-C

http://identifiers.org/hco/21/GRCh38#38055117-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94920826-C-A

38055277-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94920988-T-G

38055325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94921034-T-C

http://identifiers.org/hco/21/GRCh38#38055489-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94921178-C-A

38055524-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94921212-A-T

38055541-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94921228-A-T

38060530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94921536-G-A

38060695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94921680-G-A

38060836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94921829-G-A

38061043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94921924-G-A

38061354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94922056-C-T

38061485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94922175-G-A

38061561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94922236-T-C

38061814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94922475-C-T

38061874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94922532-A-G

38061941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94922595-G-A

38062184-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94922850-T-G

38062769-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94922999-C-G

38062770-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94923001-A-T

38062789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94923024-G-A

38062820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94923059-G-A

38063109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94923333-G-A

38063135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94923365-A-G

http://identifiers.org/hco/21/GRCh38#38063151-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94923381-C-A

38069833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94925208-G-A

38069847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94925222-C-T

38069972-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94925348-G-C

38070126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94926012-C-T

38070228-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94926110-C-G

38070251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94926134-G-A

38070349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94926239-A-G

38070414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94926312-T-C

http://identifiers.org/hco/21/GRCh38#38070489-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94926387-C-A

38070701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94927950-C-T

38070866-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94928268-A-T

38070872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94928274-G-A

http://identifiers.org/hco/21/GRCh38#38070997-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94928347-A-C

38071004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94928352-G-A

38071141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94928468-G-A

38071872-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94929114-G-C

38071945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94929187-G-A

38072026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94929276-T-C

38072057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94929316-C-T

38072101-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94929358-T-A

38072139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94929392-A-G

http://identifiers.org/hco/21/GRCh38#38077535-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94932653-A-C

http://identifiers.org/hco/21/GRCh38#38077536-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94932654-A-C

38077613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94932714-C-T

38077957-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94933072-G-T

38082061-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94933765-T-G

38082096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94933795-T-C

38082185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94933891-C-T

38082363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94934072-A-G

38082524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94934240-A-G

38082537-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94934253-C-G

38082537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94934253-C-T

38082547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94934263-C-T

38082690-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94934405-A-T

38082715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94934430-G-A

http://identifiers.org/hco/21/GRCh38#38082852-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94934525-C-A

38082853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94934526-T-C

38082868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94934538-A-G

38082890-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94934560-A-T

38082898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94934568-C-T

38082937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94934606-G-A

38083119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94934797-A-G

http://identifiers.org/hco/21/GRCh38#38089586-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94941325-A-C

38089586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94941325-A-G

38089602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94941341-T-C

http://identifiers.org/hco/21/GRCh38#38089613-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94941355-C-A

38089825-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94941525-C-G

38089825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94941525-C-T

38089942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94941629-G-A

38091778-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94942398-C-G

38091840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94942455-C-T

38091864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94942479-T-C

38091913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94942529-C-T

38091929-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94942544-T-A

http://identifiers.org/hco/21/GRCh38#38092098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94942689-C-A

38092464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94943055-G-A

38092467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94943058-G-A

38092493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94943084-G-A

38093250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94945194-G-A

38093250-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94945194-G-T

http://identifiers.org/hco/21/GRCh38#38093319-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94945263-C-A

38093319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94945263-C-T

38093324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94945268-A-G

38093327-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94945271-G-T

http://identifiers.org/hco/21/GRCh38#38093348-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94945296-C-A

38093453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94945394-G-A

38093652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94946252-T-C

38093674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94946274-A-G

38094226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94946810-G-A

38096949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94948486-A-G

38097097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94948636-G-A

38097097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94948636-G-T

38097167-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94948707-G-T

38097168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94948708-C-T

38097351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94948865-T-C

38097430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94948930-T-C

38097487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94948985-G-A

38097665-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94949163-T-A

38097970-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94949382-G-C

38097972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94949384-A-G

38099063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94949941-T-C

38099082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94949955-G-A

http://identifiers.org/hco/21/GRCh38#38099637-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#94950439-C-A

38099637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94950439-C-T

38099644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94950446-T-C

38099730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94950522-G-A

38099786-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-T

38099975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94951230-T-C

38099981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94951256-C-T

38100068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94951342-T-C

38100128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94951395-A-G

38100215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94951459-A-G

38100230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94951474-T-C

38100258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94951502-C-T

38100444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94951641-T-C

38100505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94951701-T-C

38100506-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94951702-G-T

38100567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94951762-G-A

38100838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94952199-T-C

38100881-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94952240-T-A

38100882-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94952241-G-C

38101159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94952470-G-A

38101293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94953247-G-A

38101380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94953355-T-C

38101444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94953443-C-T

38102087-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94954079-C-G

38104657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94959347-C-T

38104694-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94959380-A-T

38104796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94959498-A-G

38105156-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94959824-T-A

38105182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94959850-C-T

38105185-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94959853-T-G

38105188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94959856-C-T

38117237-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94961238-G-C

38117332-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94961321-A-T

38117388-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94961379-T-A

38117553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94961509-T-C

38117607-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94961563-G-C

38117751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94961705-A-G

38117761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94961715-C-T

38118084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94962074-G-A

38118171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94962158-C-T

38118172-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94962159-A-T

38118486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94962374-T-C

38118530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94962419-G-A

38118530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94962419-G-T

38118538-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94962427-C-G