http://identifiers.org/hco/13/GRCh38#53952498-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81268383-C-A

53952498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81268383-C-T

53952764-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81268645-G-C

53952764-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81268645-G-T

53952786-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81268666-G-C

53953264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81269135-T-C

53953275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81269146-A-G

53953486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81269321-T-C

53953495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81269330-G-A

53953552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81269386-G-A

53953771-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81269639-A-T

53953821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81269676-C-T

53953942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81269818-C-T

http://identifiers.org/hco/13/GRCh38#53954063-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81269982-C-A

53954063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81269982-C-T

53954724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81269056-G-A

53954724-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81269056-G-C

53955185-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81272088-C-G

53955195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81272095-T-C

53955195-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81272095-T-G

53955209-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81272109-T-G

53955329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: non coding transcript exon variant
orthologous variants: 81272236-C-T

53955401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81272302-G-A

53955437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81272338-C-T

53955537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81272436-A-G

53955538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81272437-G-A

53955538-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81272437-G-C

53955704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: non coding transcript exon variant
orthologous variants: 81272636-G-A

53955936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81272860-A-G

53955953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81272874-G-A

53955965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81272886-T-C

53955984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81272905-T-C

53956130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81273061-T-C

53956575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: non coding transcript exon variant
orthologous variants: 81273504-T-C

53956609-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: non coding transcript exon variant
orthologous variants: 81273538-T-G

53956635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: non coding transcript exon variant
orthologous variants: 81273564-T-C

53956770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81273699-A-G

53956902-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81273831-T-C

53957044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81273970-T-C

53957118-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81274044-G-C

http://identifiers.org/hco/13/GRCh38#53957350-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81274277-A-C

53957490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81274448-T-C

53957514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: non coding transcript exon variant
orthologous variants: 81274471-T-C

53957542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: non coding transcript exon variant
orthologous variants: 81274499-T-C

53957581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81274551-T-C

53957826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81274822-C-T

53957848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81274844-A-G

53957897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81274882-G-A

53957900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81274885-T-C

http://identifiers.org/hco/13/GRCh38#53958109-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81275098-A-C

53959158-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81276219-C-G

53959158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81276219-C-T

http://identifiers.org/hco/13/GRCh38#53959180-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81276240-A-C

53959226-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81276285-G-T

53959352-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81276399-T-A

53959399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81276445-A-G

53959496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81276531-T-C

53959573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81276596-C-T

53959580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81276603-A-G

53984455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81285395-G-A

53984456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81285396-A-G

http://identifiers.org/hco/13/GRCh38#53984616-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81285498-C-A

53984673-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81285558-C-G

53984843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81285728-T-C

53985149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81286434-T-C

53985192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81286458-T-C

http://identifiers.org/hco/13/GRCh38#53985307-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81286576-C-A

53985325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81286595-G-A

53985639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81286926-G-A

http://identifiers.org/hco/13/GRCh38#53985800-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81287164-C-A

53985800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81287164-C-T

53986045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81287414-G-A

53986098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81287467-T-C

53986121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81287490-C-T

53986235-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81287600-C-G

http://identifiers.org/hco/13/GRCh38#53986282-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81287648-C-A

http://identifiers.org/hco/13/GRCh38#53987303-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81290055-C-A

53987305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81290060-T-C

53987310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81290065-T-C

53987365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81290102-A-G

53987605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81290350-G-A

53987749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81290477-T-C

53987772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81290499-C-T

http://identifiers.org/hco/13/GRCh38#53987896-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81290945-C-A

53987942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81290993-T-C

53988032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81291080-G-A

http://identifiers.org/hco/13/GRCh38#53988260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81291315-C-A

53988261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81291316-A-G

53989070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81294749-G-A

53989097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81294776-A-G

53989099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81294778-A-G

53989128-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81294806-T-G

53989199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81294871-C-T

53989207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81294879-A-G

53989288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81294955-A-G

http://identifiers.org/hco/13/GRCh38#53989311-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81294979-A-C

53989594-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81295274-T-A

53989896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81295466-G-A

http://identifiers.org/hco/13/GRCh38#53990281-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81295844-A-C

http://identifiers.org/hco/13/GRCh38#53990707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81296757-C-A

53990707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81296757-C-T

53990817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81296866-A-G

53990879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81296928-C-T

http://identifiers.org/hco/13/GRCh38#53990982-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81297035-C-A

53991071-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81297114-C-G

53991354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81297494-A-G

http://identifiers.org/hco/13/GRCh38#53991421-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81297580-C-A

53991463-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81297616-T-A

53991463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81297616-T-C

53991673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81297816-G-A

53991898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81298019-G-A

53991912-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81298031-G-C

53991912-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81298031-G-T

53992298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81298405-G-T

53992861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81298900-G-A

http://identifiers.org/hco/13/GRCh38#53992891-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81298930-C-A

53992923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81298948-G-A

53992923-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81298948-G-C

53993031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81299051-A-G

http://identifiers.org/hco/13/GRCh38#53993073-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81299089-A-C

53997842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81306262-T-C

53998042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81306460-T-C

53998081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81306528-G-A

53998081-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81306528-G-T

53998161-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81306607-G-C

53998512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81306968-A-G

53998556-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81306999-T-G

53999180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81308239-C-T

53999452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81308485-A-G

53999565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81308628-G-A

53999565-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81308628-G-C

http://identifiers.org/hco/13/GRCh38#53999683-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81308764-A-C

http://identifiers.org/hco/13/GRCh38#53999795-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81308886-C-A

53999878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81308949-A-G

http://identifiers.org/hco/13/GRCh38#53999937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81309002-C-A

53999937-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81309002-C-G

54000006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81309071-A-G

http://identifiers.org/hco/13/GRCh38#54000008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81309073-C-A

54000270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81309295-A-G

54000384-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81309341-T-A

54000445-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81309411-T-A

54000445-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81309411-T-C

54000565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81309535-C-T

54000839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81309783-G-A

54000922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81309868-T-C

http://identifiers.org/hco/13/GRCh38#54000935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81309880-C-A

54001153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81310080-A-G

54001169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81310096-C-T

54003548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81311453-G-A

54003692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81311579-G-A

54003889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81311782-A-G

54003991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81311878-A-G

54004263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81312205-T-C

54004478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81312545-C-T

54004520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81312587-A-G

54004535-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81312602-T-A

54005252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81313401-A-G

54005252-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81313401-A-T

54005566-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81314304-T-A

54005573-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81314311-T-G

54005777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81314499-C-T

54005872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81314598-A-G

54005921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81314648-G-A

54005998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81314725-G-A

54006142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81314868-G-A

54006184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81314911-G-A

54006184-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81314911-G-C

54006199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81314926-C-T

54006231-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81314956-T-G

54006314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81315039-G-A

54006590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81315300-G-A

54006590-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81315300-G-C

54006599-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81315309-G-C

54006833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81315595-T-C

http://identifiers.org/hco/13/GRCh38#54006840-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81315602-C-A

54007044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81315725-A-G

54007369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81316740-G-A

54007392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81316767-G-A

54007886-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81317021-A-T

54007917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81317047-C-T

54008033-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81317151-G-C

54008044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81317162-C-T

54008060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81317178-T-C

http://identifiers.org/hco/13/GRCh38#54008106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81317229-C-A

54008192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81317285-G-A

54010237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81317971-T-C

http://identifiers.org/hco/13/GRCh38#54010386-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81318119-A-C

54010468-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81318202-T-G

54010521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81318254-C-T

54010523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81318261-A-G

54010579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81318294-G-A

54010878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81321488-C-T

54010975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81321580-G-A

54011006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81321608-G-A

54015019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81334945-T-C

54015102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81335027-G-A

54015302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81335231-C-T

54015833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81335454-A-G

54016151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81335790-G-A

54016151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81335790-G-T

54016411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81335895-G-A

54016479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81335969-T-C

54016493-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81335983-A-T

http://identifiers.org/hco/13/GRCh38#54016551-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81336041-C-A

54016619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81336110-G-A

54017536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81337019-C-T

http://identifiers.org/hco/13/GRCh38#54018368-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81337500-A-C

54018368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81337500-A-G

54018390-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81337512-T-G

54018603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81337685-C-T

http://identifiers.org/hco/13/GRCh38#54018722-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81337794-C-A

54018722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81337794-C-T

54018937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81337992-C-T

54018940-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81337995-T-A

54018975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81338009-C-T

54019051-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81338084-C-G

54019133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81338165-C-T

54019134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81338166-C-T

54019237-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81338258-T-A

54019246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81338267-T-C

54019356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81338514-C-T

54019380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81338538-T-C

54019483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81338639-T-C

54019483-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81338639-T-G

http://identifiers.org/hco/13/GRCh38#54019574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81338728-C-A

http://identifiers.org/hco/13/GRCh38#54019912-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81339021-C-A

54020046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81339138-C-T

54020099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81339198-A-G

http://identifiers.org/hco/13/GRCh38#54020347-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81339410-A-C

54020618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81339679-G-A

54020892-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81339953-A-T

54021082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81340119-A-G

54027728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81342296-G-A

54027728-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81342296-G-C

54027934-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81342499-C-G

54027934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81342499-C-T

54027955-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81342520-C-G

54027978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81342543-T-C

54027994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81342559-T-C

54028021-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81342585-G-C

54028181-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81342744-T-A

54028324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81342875-G-A

http://identifiers.org/hco/13/GRCh38#54028424-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81342977-A-C

54028523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81343069-T-C

54028628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81343161-T-C

http://identifiers.org/hco/13/GRCh38#54028678-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81343204-A-C

54028885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81343408-G-A

54028910-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81343429-T-A

54028910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81343429-T-C

54028963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81343484-T-C

54028970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81343491-A-G

http://identifiers.org/hco/13/GRCh38#54029043-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81343559-A-C

54029059-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81343574-C-G

54029215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81343767-C-T

54029263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81343806-T-C

54029324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81343867-G-A

54029347-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81343890-G-C

54029670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81345127-C-T

54029885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81345469-A-G

54029889-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81345473-T-G

54029929-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81345535-T-G

54029963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81345569-G-A

54030119-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81345748-G-T

54030444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81346036-A-G

54030444-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81346036-A-T

54030729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81346263-C-T

54030764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81346297-A-G

54030764-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81346297-A-T

54042421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81363289-C-T

54042462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81363330-C-T

54042781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81363614-A-G

54042813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81363646-T-C

54042813-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81363646-T-G

54050582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81365331-T-C

54050612-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81365360-G-C

54050811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81365563-G-A

54050811-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81365563-G-T

54051023-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81365772-T-A

54051056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81365806-A-G

54051057-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81365807-T-C

54051076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81365827-G-A

54051290-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81366422-A-T

http://identifiers.org/hco/13/GRCh38#54051568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81367113-C-A

54051636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81367157-G-A

54052230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81367683-A-G

54052288-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81367754-T-G

http://identifiers.org/hco/13/GRCh38#54052305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81367768-C-A

54052592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81371888-A-G

54052701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81371993-G-A

http://identifiers.org/hco/13/GRCh38#54052752-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81372030-A-C

54052752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81372030-A-G

54052794-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81372072-A-T

54054752-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81373346-C-G

54054987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81373568-T-C

54055235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81374320-C-T

http://identifiers.org/hco/13/GRCh38#54055630-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81374457-C-A

54055944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81374756-A-G

54056001-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81374815-C-G

54056024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81374838-A-G

54056217-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81375015-C-G

54056418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81375189-G-A

54056447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81375221-C-T

54056645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81375415-G-A

54058027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81377553-A-G

54058138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81377666-C-T

54058489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81378044-A-G

54060358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81378540-T-C

54060365-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81378547-A-T

54060378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81378560-T-C

http://identifiers.org/hco/13/GRCh38#54061660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81379254-C-A

54061831-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81379415-T-A

54063102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81380229-G-A

54063169-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81380296-T-G

54063281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81380408-C-T

54063495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81380558-T-C

54063810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81380825-T-C

http://identifiers.org/hco/13/GRCh38#54063840-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81380855-C-A

54063922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81380931-T-C

54063923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81380932-T-C

http://identifiers.org/hco/13/GRCh38#54063977-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81381876-C-A

54064024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81381922-A-G

54064077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81381982-G-A

http://identifiers.org/hco/13/GRCh38#54064232-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81382125-C-A

54064240-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81382133-T-A

54069426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81389798-G-A

54069566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81389941-C-T

54069579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81389954-A-G

54073044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81396045-G-A

54073044-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81396045-G-T

54073476-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81396486-C-G

54073627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81396633-G-T

54073741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81396744-C-T

54073756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81396759-T-C

54073785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81396787-G-A

54074496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81398272-T-C

54074577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81398380-A-G

54074847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81398651-G-A

54074862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81398678-C-T

54074871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81398687-A-G

54075022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81398830-C-T

54075214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81399137-T-C

54078935-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81400781-C-G

54079151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81400983-C-T

54079338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81401179-A-G

54079395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81401213-T-C

54079430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81401250-A-G

http://identifiers.org/hco/13/GRCh38#54079666-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81401676-C-A

54079666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81401676-C-T

54079672-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81401682-C-G

54079687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81401698-A-G

54079971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81401964-T-C

54080453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81402421-C-T

54080666-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81402617-T-G

http://identifiers.org/hco/13/GRCh38#54080713-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81402664-C-A

54080713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81402664-C-T

54080795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81402729-G-A

54081009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81403102-A-G

54081086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81403176-C-T

54081158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81403253-T-C

54082547-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81403464-T-G

54082591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81403506-C-T

http://identifiers.org/hco/13/GRCh38#54082621-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81403533-C-A

54082694-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81403605-G-C

54082940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81403834-A-G

54082956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81403850-A-G

54083437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81404329-T-C

54083714-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81404587-C-G

54083793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81405249-C-T

54083807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81405262-A-G

54083858-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81405306-G-T

54083863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81405311-G-A

54083874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81405322-A-G

54084465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81405880-C-T

54084713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81406178-G-A

54084862-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81406326-A-T

http://identifiers.org/hco/13/GRCh38#54084895-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81406359-A-C

54085008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81406471-C-T

54085295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81406748-T-C

54095713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81407506-C-T

54095715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81407508-C-T

54095835-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81407616-G-T

54095896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81407676-A-G

54096077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81407855-C-T

54096179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81407954-C-T

54096200-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81407976-T-A

54096372-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81408135-G-T

54096416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81408179-T-C

http://identifiers.org/hco/13/GRCh38#54096827-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81408561-A-C

54099340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81420830-C-T

54099415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81420907-C-T

54099425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81420917-T-C

54099438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81420930-T-C

54099453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81420949-C-T

54099551-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81421019-T-G

http://identifiers.org/hco/13/GRCh38#54099650-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81421121-C-A

54099655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81421126-G-A

54099961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81421425-C-T

54099962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81421426-G-A

54099971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81421435-G-A

54100127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81421590-C-T

54100290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81421754-G-A

http://identifiers.org/hco/13/GRCh38#54101007-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81422419-A-C

54101025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81422440-G-A

http://identifiers.org/hco/13/GRCh38#54101028-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81422443-C-A

54101028-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81422443-C-G

54101086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81422533-G-A

54101087-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81422534-T-C

54101218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81422698-C-T

54101242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81422720-T-C

http://identifiers.org/hco/13/GRCh38#54101300-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81422772-A-C

54101345-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81422815-T-G

54101520-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81422979-A-T

54105851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81423568-C-T

http://identifiers.org/hco/13/GRCh38#54105909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81423626-C-A

54106136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81423865-G-A

http://identifiers.org/hco/13/GRCh38#54106221-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81423954-A-C

54106385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81424091-C-T

http://identifiers.org/hco/13/GRCh38#54106413-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81424119-C-A

http://identifiers.org/hco/13/GRCh38#54106420-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81424126-C-A

54107049-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81424313-C-G

54107129-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81424371-A-T

54107146-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81424389-T-G

54107228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81424458-G-A

54107278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81424503-A-G

54107284-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81424509-C-G

54107303-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81424528-G-T

http://identifiers.org/hco/13/GRCh38#54107552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81427201-C-A

54107583-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81427232-C-G

54107839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81427479-A-G

54107850-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81427490-T-G

http://identifiers.org/hco/13/GRCh38#54107867-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81427507-C-A

54109788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81428894-C-T

54110464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81429436-G-A

54110536-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81429508-C-G

54110536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81429508-C-T

54110733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81429705-A-G

54111033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81429994-G-A

54111036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81429997-G-A

54111090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81430048-A-G

54111491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81430431-A-G

54111491-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81430431-A-T

54112172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81430742-G-A

54112353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81430906-T-C

54112364-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81430917-T-G

54112591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81431074-C-T

http://identifiers.org/hco/13/GRCh38#54112811-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81431286-C-A

54112838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81431310-C-T

54112925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81431564-C-T

54113123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81431759-T-C

54113123-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81431759-T-G

54113180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81431816-T-C

54113275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81431909-T-C

54113344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81431972-C-T

http://identifiers.org/hco/13/GRCh38#54113458-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81432086-A-C

54113493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81432118-T-C

54113498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81432123-C-T

54113613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81432215-G-A

54114163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81432680-C-T

54114296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81432815-G-A

54114312-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81432831-G-C

54114430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81432930-C-T

54114446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81432946-T-C

54114642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81433137-C-T

http://identifiers.org/hco/13/GRCh38#54114779-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81433243-C-A

54114779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81433243-C-T

54114815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81433270-A-G

54114819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81433274-G-T

54115088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81433530-A-G

54115169-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81433599-G-C

54115331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81433729-C-T

54115332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81433730-G-A

54115396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81433794-G-A

54115396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81433794-G-T

54115511-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81433870-C-G

54115821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81434166-G-A

54115858-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81434206-T-G

54115874-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81434227-A-T

54115877-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81434230-G-T

54115951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81434319-C-T

54115952-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81434320-C-G

http://identifiers.org/hco/13/GRCh38#54115966-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81434334-C-A

54115966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81434334-C-T

54115982-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81434358-G-T

54116041-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81434425-G-T

54116059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81434442-G-A

54116060-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81434443-G-C

54116060-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81434443-G-T

54116101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81434472-T-C

54116109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81434480-G-A

54116154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81434509-G-A

54116165-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81434520-T-A

54116187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81434536-C-T

54116198-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81434553-C-G

54116247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81434626-G-A

http://identifiers.org/hco/13/GRCh38#54116251-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81434637-C-A

54116257-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81434643-G-T

http://identifiers.org/hco/13/GRCh38#54116275-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81434663-C-A

54116275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81434663-C-T

54116281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81434669-A-G

54116289-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81434677-A-T

54116290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81434678-G-A

54116290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81434678-G-T

54116292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81434680-A-G

http://identifiers.org/hco/13/GRCh38#54116341-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81434723-C-A

54116367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81434747-G-A

54116367-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81434747-G-T

54116379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81434759-A-G

54116398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81434778-A-G

54116539-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81434903-G-T

54116547-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81434911-G-T

http://identifiers.org/hco/13/GRCh38#54118349-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81436938-A-C

54118519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81437093-G-A

54119123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81437665-T-C

54119125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81437667-T-C

54119182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81437723-G-A

54119212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81437750-A-G

54119265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81437816-C-T

54119292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81437852-G-A

54119322-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81437879-C-G

54119326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81437883-T-C

54119368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81437920-C-T

54119438-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81437970-T-A

54119630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81438154-G-A

http://identifiers.org/hco/13/GRCh38#54119646-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81438166-C-A

54119922-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: -G-T

54119952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: -T-C

54120005-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: -T-A

54120028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: -T-C

54120081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: -G-A

54121537-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81446022-T-G

54121591-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81446063-A-T

54121628-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81446100-T-G

54121690-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81446164-T-G

54122014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81446493-A-G

http://identifiers.org/hco/13/GRCh38#54122157-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81446643-C-A

54122171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81446658-C-T

54123238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81447090-G-A

54123252-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81447104-G-T

54123380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81447226-G-A

54123421-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81447267-G-T

54123483-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81447324-T-A

54123594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81447438-G-A

54123594-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81447438-G-C

http://identifiers.org/hco/13/GRCh38#54123614-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81447458-C-A

54123737-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81447580-T-G

54123760-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81447601-G-T

http://identifiers.org/hco/13/GRCh38#54123879-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81447707-C-A

54123905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81447733-T-C

54124395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81448229-T-C

54126234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81448319-A-G

54126235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81448320-T-C

54126578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81448629-G-A

54126578-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81448629-G-C

54126588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81448639-T-C

54126591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81448642-G-A

http://identifiers.org/hco/13/GRCh38#54126755-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81448752-C-A

54126755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81448752-C-T

54126756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81448753-A-G

54126756-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81448753-A-T

54126784-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81448780-G-T

http://identifiers.org/hco/13/GRCh38#54126806-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81448802-C-A

http://identifiers.org/hco/13/GRCh38#54126808-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81448804-C-A

54126841-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81448837-T-G

54126911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81448945-T-C

54127048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81449111-T-C

54127114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81449172-G-A

54127163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81449214-G-T

54127377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81449414-A-G

54127377-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81449414-A-T

54127382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81449419-G-A

54127382-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81449419-G-C

http://identifiers.org/hco/13/GRCh38#54127386-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81449423-C-A

54127386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81449423-C-T

54133303-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81449586-G-C

54133320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81449602-T-C

54133350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81449632-C-T

54133784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81450015-A-G

54133803-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81450037-T-G

http://identifiers.org/hco/13/GRCh38#54134012-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81450248-A-C

54134082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81450314-T-C

http://identifiers.org/hco/13/GRCh38#54134162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81450384-C-A

54134323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81450553-C-T

54135293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81450737-A-G

54135414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81450972-G-A

54135431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81451048-G-A

54135549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81451174-G-A

54135549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81451174-G-T

http://identifiers.org/hco/13/GRCh38#54135580-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81451206-C-A

54135580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81451206-C-T

54135666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81451289-T-C

54135890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81451504-A-G

54135893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81451507-C-T

54135921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81451561-C-T

54135939-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81451579-C-G

54136290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81452415-G-T

54136299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81452424-A-G

54136457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81452552-T-C

54136562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81452644-C-T

http://identifiers.org/hco/13/GRCh38#54136607-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81452692-A-C

54136690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81452771-T-C

54136723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81452804-G-A

http://identifiers.org/hco/13/GRCh38#54136749-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81452830-C-A

54136749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81452830-C-T

54136777-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81452848-T-G

54136778-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81452849-G-C

http://identifiers.org/hco/13/GRCh38#54136999-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81453084-C-A

54136999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81453084-C-T

54137169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81453293-C-T

54137220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81453343-C-T

54137394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81453949-A-G

54137407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81453975-T-C

54137420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81453988-A-G

54137567-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81454241-C-G

54137688-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81454359-G-C

54137699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81454370-C-T

http://identifiers.org/hco/13/GRCh38#54137707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81454378-C-A

http://identifiers.org/hco/13/GRCh38#54137737-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81454408-C-A

54138036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81454524-G-A

http://identifiers.org/hco/13/GRCh38#54138163-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81454632-C-A

54138198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81454671-T-C

54138661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81454872-C-T

54138702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81454914-C-T

54138717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81454929-T-C

54138767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81454970-A-G

54138782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81454985-T-C

54141761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81455572-T-C

http://identifiers.org/hco/13/GRCh38#54141794-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81455604-A-C

54142018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81455810-C-T

http://identifiers.org/hco/13/GRCh38#54142321-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81456092-C-A

54142428-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81456186-C-G

54142504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81456257-A-G

54142592-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81456346-T-G

54142612-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81456366-C-G

54142668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81456415-T-C

54142802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81456568-G-A

54142818-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81456584-G-C

54142943-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81456666-G-C

54143140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81456840-T-C

54143254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81458035-C-T

54143272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81458045-T-C

54143320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81458095-A-G

54143404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81458151-T-C

54143404-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81458151-T-G

54143410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81458157-G-A

54143516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81458271-C-T

http://identifiers.org/hco/13/GRCh38#54143804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81458533-C-A

54143846-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81458569-G-T

54143850-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81458573-C-G

54143877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81458587-C-T

54143935-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81458642-T-G

54144040-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81458736-G-C

54145310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81459588-C-T

54145467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81459748-T-C

http://identifiers.org/hco/13/GRCh38#54145477-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81459758-A-C

54146005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81460203-T-C

54146026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81460224-G-T

54146179-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81460355-A-T

http://identifiers.org/hco/13/GRCh38#54146418-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81460594-A-C

http://identifiers.org/hco/13/GRCh38#54146439-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81460615-A-C

54146696-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81460816-T-G

54146697-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81460817-G-T

54146867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81460980-C-T

54146871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81460983-T-C

54146880-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81460992-C-G

54146963-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81461077-T-A

54147114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81461213-G-A

54147163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81461263-T-C

http://identifiers.org/hco/13/GRCh38#54147219-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81461303-C-A

54147229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81461313-C-T

54147230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81461314-G-A

54147230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81461314-G-T

54153106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81466409-C-T

54153158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81466460-G-T

54153891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81467121-G-A

54153906-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81467136-T-A

54153953-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81467183-G-T

http://identifiers.org/hco/13/GRCh38#54154186-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81467428-A-C

54154209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81467451-A-G

54154209-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81467451-A-T

54154273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81467513-G-A

54154447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81467676-G-A

54154476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81467698-A-G

54155090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81468307-A-G

54155105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81468325-T-C

http://identifiers.org/hco/13/GRCh38#54155201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81468417-C-A

54155389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81468620-T-C

54155420-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81468652-A-T

54155501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81468744-G-A

54155539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81468774-G-A

54155558-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81468798-T-A

54155558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81468798-T-C

54155568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81468808-G-A

54155568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81468808-G-T

54155659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81468904-T-C

54155752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81468987-C-T

54155830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81469059-T-C

54155875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81469098-T-C

54155938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81469164-T-C

54155939-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81469165-A-G

54156013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81469237-A-G

54156094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81470187-T-C

54156213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81470307-T-C

54156221-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81470315-G-T

54156229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81470323-C-T

54156412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81470549-T-C

54157025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81470592-G-A

54157059-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81470624-T-A

54157198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81470780-A-G

54157275-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81470861-T-A

54158189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81471561-G-A

54158261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81471647-T-C

54158313-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81471696-C-G

54158342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81471710-A-G

54158371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81471736-C-T

54158379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81471744-C-T

54158694-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81472072-C-G

54158694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81472072-C-T

54159161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81472227-A-G

54159179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81472245-T-C

54159234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81472293-T-C

54159373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81472422-G-A

54159551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81472589-C-T

54159771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81472799-G-A

54159798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81472825-G-A

54160121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81473137-T-C

54160489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81473484-G-T

54160671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81473616-C-T

54160792-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81473742-T-A

54160877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81473834-T-C

54160898-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81473845-T-A

54163952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81475017-G-A

http://identifiers.org/hco/13/GRCh38#54164201-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81475268-A-C

54164233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81475302-C-T

54164416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81475484-C-T

54164479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81475905-G-A

54164531-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81475942-A-T

54164639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81476047-A-G

54164727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81476131-T-C

54164729-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81476133-C-G

54164739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81476143-A-G

54164775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81476178-T-C

54164832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81476235-G-A

54165168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81477360-C-T

54165483-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81477732-C-G

54165483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81477732-C-T

54165680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81477932-G-A

54165705-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81477957-G-T

54166016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81478275-C-T

54166296-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81478546-T-G

54166383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81478633-A-G

54166643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81478871-T-C

54166798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81479012-A-G

54166892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81481712-C-T

54166893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81481713-T-C

54166894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81481714-G-A

54166905-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81481725-C-G

54167020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81481840-T-C

54167264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81482061-G-A

http://identifiers.org/hco/13/GRCh38#54167367-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81482163-A-C

http://identifiers.org/hco/13/GRCh38#54167429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81482238-C-A

54167454-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81482263-T-A

54167460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81482273-A-G

54167594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81483361-A-G

http://identifiers.org/hco/13/GRCh38#54167696-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81483456-A-C

54167844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81483585-C-T

54168290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81484009-G-A

54168290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81484009-G-T

54168395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81484105-G-A

54168487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81484198-T-C

54168611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81484308-T-C

54173858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81487743-C-T

http://identifiers.org/hco/13/GRCh38#54173881-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81487766-A-C

54173881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81487766-A-G

54174062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81487943-C-T

54174092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81487973-G-A

54174154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81488034-G-A

54174513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81488396-A-G

54174525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81488408-A-G

54174525-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81488408-A-T

54175017-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81488859-C-G

http://identifiers.org/hco/13/GRCh38#54175476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81489257-C-A

54175476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81489257-C-T

54175535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81489312-C-T

54175560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81489337-C-T

54175689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81489443-A-G

54175689-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81489443-A-T

54176340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81489576-G-A

54176675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81489866-C-T

54176738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81489965-C-T

54176830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81490056-G-A

http://identifiers.org/hco/13/GRCh38#54177332-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81490302-A-C

54177332-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81490302-A-T

54177550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81490549-T-C

54177603-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81490640-T-A

54177684-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81490712-A-T

54177771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81490813-C-T

54177972-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81490987-T-G

54177998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81491000-C-T

54178161-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81491165-G-C

54178222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81491197-C-T

54178231-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81491203-G-C

54178236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81491208-T-C

54178246-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81491214-T-A

54178336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81491303-T-C

54178466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81491433-C-T

54178498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81491463-T-C

54178623-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81491574-T-G

http://identifiers.org/hco/13/GRCh38#54178644-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81491595-A-C

54178711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81491659-T-C

54179393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81492334-G-T

54179526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81492458-A-G

54179690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81492609-T-C

54182349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81493020-G-A

54182951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81493583-A-G

54183238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81493868-C-T

54183395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81494016-A-G

54183545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81494163-C-T

54183907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81494522-G-A

54184034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81495207-C-T

http://identifiers.org/hco/13/GRCh38#54184099-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81495272-C-A

54184099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81495272-C-T

54184127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81495300-T-C

http://identifiers.org/hco/13/GRCh38#54184756-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81496073-C-A

54184756-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81496073-C-G

54184756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81496073-C-T

http://identifiers.org/hco/13/GRCh38#54184817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81496139-C-A

54184817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81496139-C-T

54185061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81496379-G-A

54185322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81496680-C-T

54185328-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81496686-C-G

54185328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81496686-C-T

54185344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81496702-G-A

54185344-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81496702-G-T

http://identifiers.org/hco/13/GRCh38#54185413-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81496792-C-A

54185413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81496792-C-T

54185424-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81496799-G-C

54185469-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81496848-C-G

54185519-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81496894-C-G

54185519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81496894-C-T

54185555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81496909-T-C

54188162-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81497198-A-T

54188225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81497262-T-C

http://identifiers.org/hco/13/GRCh38#54188237-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81497274-C-A

54188427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81497469-A-G

http://identifiers.org/hco/13/GRCh38#54188516-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81497550-C-A

54188517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81497551-C-T

54188525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81497559-T-C

54188792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81497852-A-G

54189035-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81500324-T-A

54189271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81500626-C-T

54189374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81500794-G-T

54189429-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81500844-A-T

http://identifiers.org/hco/13/GRCh38#54189435-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81500849-A-C

54189504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81500914-T-C

54189714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81501096-A-G

http://identifiers.org/hco/13/GRCh38#54189796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81501168-C-A

54189796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81501168-C-T

54189917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81501268-T-C

54189917-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81501268-T-G

54189933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81501283-A-G

54192860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81503702-C-T

54193159-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81503998-T-G

54193739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81504575-T-C

54193748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81504584-A-G

54193922-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81504767-A-T

54193959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81504801-C-T

54194234-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81505081-T-A

54194316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81505173-C-T

54194338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81505195-T-C

http://identifiers.org/hco/13/GRCh38#54194795-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81505652-A-C

54195029-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81505925-A-T

54195101-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81505979-C-G

54195101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81505979-C-T

54195183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81506026-T-C

54195296-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81506147-G-C

54195405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81506254-T-C

54196134-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81507000-T-G

54196181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81507047-G-A

54196181-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81507047-G-C

54196186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81507052-T-C

54196527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81507408-C-T

54197068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81509082-A-G

http://identifiers.org/hco/13/GRCh38#54197171-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81509165-C-A

54198656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81510164-T-C

54198659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81510167-G-A

54198717-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81510235-A-T

54198803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81510311-C-T

54199039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-G

54199045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-C

54199045-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-G

54199114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

54199152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

54199209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81511289-C-T

http://identifiers.org/hco/13/GRCh38#54199384-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81511492-C-A

54199384-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81511492-C-G

54199384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81511492-C-T

54199385-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81511493-C-G

54199407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81511560-C-T

54199474-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81511641-C-G

54199474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81511641-C-T

54199902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81511979-G-A

54200195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81512269-G-A

54200258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81512345-T-C

54200451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81512528-G-T

http://identifiers.org/hco/13/GRCh38#54200484-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81512562-C-A

54200969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81513045-G-A

54200985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81513061-T-C

54203513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81519039-T-C

54203643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81519157-G-A

54203776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81519258-C-T

54203808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81519314-G-A

54203808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81519314-G-T

54204030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81519494-G-A

54204132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81519616-G-A

54204275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81519750-T-C

54204278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81519753-C-T

54204500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81519911-G-A

54204500-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81519911-G-C

54204990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81520045-C-T

54205028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81520085-T-C

http://identifiers.org/hco/13/GRCh38#54205121-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81520177-A-C

54205121-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81520177-A-T

54205596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81520667-C-T

54205763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81520832-T-C

54205804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81520867-G-A

54206038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81521258-C-T

54206047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81521267-C-T

54206062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81521280-A-G

54206062-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81521280-A-T

54206307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81521691-T-C

54206307-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81521691-T-G

54206331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81521716-G-A

54206622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81522001-T-C

54206662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81522038-C-T

54206739-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81522107-G-T

54206778-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81522161-C-G

54206855-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81522231-G-T

54208166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81523222-T-C

54208391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81523430-A-G

54208660-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81524488-T-A

54208788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81524595-A-G

54208805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81524612-T-C

54208907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81524801-T-C

54209030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81524924-G-A

54209134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81525033-A-G

54209264-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81525164-T-A

http://identifiers.org/hco/13/GRCh38#54209309-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81525209-C-A

http://identifiers.org/hco/13/GRCh38#54209496-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81525403-A-C

54209670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81525579-C-T

54209855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81525757-G-A

54209874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81525776-G-A

54212511-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81528739-A-T

http://identifiers.org/hco/13/GRCh38#54212524-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81528753-A-C

54212528-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81528757-C-G

54212943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81529233-G-A

http://identifiers.org/hco/13/GRCh38#54213009-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81529279-A-C

54213031-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81529300-T-A

54213031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81529300-T-C

54213067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81529335-T-C

54213216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81529485-C-T

54214804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81531066-A-G

54214939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81531208-G-A

54214954-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81531340-T-A

54215049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81531470-G-A

54215071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81531491-T-C

54215566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81531640-A-G

54228886-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81532883-C-G

54228886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81532883-C-T

54228940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81532939-A-G

54229463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81533866-T-C

54229519-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81533913-T-G

54229795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81534780-C-T

54229805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81534790-A-G

54229943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81534952-C-T

54229996-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81535005-A-T

54230373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81535347-G-A

http://identifiers.org/hco/13/GRCh38#54230404-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81535379-C-A

54230439-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81535411-C-G

54230439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81535411-C-T

54230444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81535416-T-C

54230539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81535476-G-A

54230539-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81535476-G-C

54230655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81535585-T-C

54230678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81535603-G-T

54230967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81535878-A-G

54231625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81536543-C-T

http://identifiers.org/hco/13/GRCh38#54232154-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81538612-C-A

54232154-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81538612-C-G

54232205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81538663-T-C

54232250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81538708-T-C

54232351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81538818-G-A

54232364-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81538831-A-T

54232513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81538967-G-A

http://identifiers.org/hco/13/GRCh38#54232555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81539017-C-A

54232721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81539158-A-G

54232743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81539180-C-T

54232762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81539199-T-C

54232870-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81539305-T-G

54241629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81544453-A-G

54241776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81544644-T-C

54242015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81544888-C-T

54242022-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81544895-G-T

54242246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81545110-T-C

54242400-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81545262-T-A

54242556-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81545409-G-C

54242556-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81545409-G-T

54245849-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81546362-T-G

http://identifiers.org/hco/13/GRCh38#54245898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81546409-C-A

54245901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81546411-T-C

http://identifiers.org/hco/13/GRCh38#54245993-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81546499-A-C

54245993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81546499-A-G

54246049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81546552-C-T

54246076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81546579-G-A

http://identifiers.org/hco/13/GRCh38#54246113-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81546601-C-A

54246113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81546601-C-T

54246280-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81546756-A-T

54246340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81546822-A-G

54246419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81546898-C-T

54246880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81547274-T-C

54246881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81547275-G-A

http://identifiers.org/hco/13/GRCh38#54246956-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81547359-A-C

54247083-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81547486-A-T

54247173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81547600-T-C

54247542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81547935-T-C

54247603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81547993-G-A

54247603-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81547993-G-T

54248408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81548435-G-A

54248730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81548764-T-C

54250826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81552218-A-G

54250899-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81552289-A-T

http://identifiers.org/hco/13/GRCh38#54250971-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81552357-A-C

54250971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81552357-A-G

54251257-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81552652-G-T

54251562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81552959-G-A

http://identifiers.org/hco/13/GRCh38#54251706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81553099-C-A

54251761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81553162-T-C

54251792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81553202-C-T

54251826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81553236-T-C

54251863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81553269-G-A

54251934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81553344-C-T

54251998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81553401-C-T

54252028-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81553430-T-A

54252334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81553715-A-G

54253999-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81555572-T-A

54254090-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81555660-G-T

http://identifiers.org/hco/13/GRCh38#54254444-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81555958-A-C

54254445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81555959-C-T

54254446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81555960-T-C

54254640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81556148-G-A

54254745-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81556251-G-T

54254788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81556295-G-A

http://identifiers.org/hco/13/GRCh38#54254884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81556388-C-A

54254884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81556388-C-T

54254912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81556415-T-C

54255000-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81561342-G-T

54255021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81561359-C-T

54255035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81561372-C-T

54255389-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81561647-T-G

54256024-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81562266-T-C

http://identifiers.org/hco/13/GRCh38#54264601-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#81567305-C-A

54264793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81567499-T-C

54264907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81567621-A-G

54265038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81567727-G-A