http://identifiers.org/hco/10/GRCh38#12068956-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#5947578-C-A

12068956-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 5947578-C-G

12068956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 5947578-C-T

12068984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 5947544-G-A

12068984-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 5947544-G-C

12069041-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: missense_variant, undefined
orthologous variants: 5947470-C-G

12069041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: missense_variant, undefined
orthologous variants: 5947470-C-T

12069046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: missense_variant, undefined
orthologous variants: 5947465-A-G

http://identifiers.org/hco/10/GRCh38#12069056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: missense_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#5947455-C-A

12069098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: missense_variant, undefined
orthologous variants: 5947413-G-A

12069098-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: missense_variant, undefined
orthologous variants: 5947413-G-C

12069150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: synonymous_variant, undefined
orthologous variants: 5947361-G-A

12069150-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: missense_variant, undefined
orthologous variants: 5947361-G-C

http://identifiers.org/hco/10/GRCh38#12069160-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: missense_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#5947351-C-A

12069161-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: missense_variant, undefined
orthologous variants: 5947350-C-G

12069161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: missense_variant, undefined
orthologous variants: 5947350-C-T

12069170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: missense_variant, undefined
orthologous variants: 5947341-C-T

http://identifiers.org/hco/10/GRCh38#12069230-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#5947292-C-A

12069230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5947292-C-T

http://identifiers.org/hco/10/GRCh38#12069236-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#5947286-C-A

12069236-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5947286-C-G

12069236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5947286-C-T

12069270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron_variant, undefined
orthologous variants: 5947260-T-C

12069270-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron_variant, undefined
orthologous variants: 5947260-T-G

12069468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5947061-C-T

http://identifiers.org/hco/10/GRCh38#12069566-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#5946908-A-C

http://identifiers.org/hco/10/GRCh38#12069654-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#5946817-C-A

12069719-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5946719-G-T

12069728-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5946710-G-C

12069728-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5946710-G-T

12069753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5946685-G-A

12069791-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5946628-G-C

12069797-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5946622-C-G

12072186-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5941860-C-G

12072186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5941860-C-T

12072227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5941819-G-A

12072280-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5941746-G-C

http://identifiers.org/hco/10/GRCh38#12072416-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#5941633-C-A

12072417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5941632-A-G

12081416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5937401-G-A

12081416-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5937401-G-T

12081447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5937370-A-G

12081543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5937280-C-T

12081549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5937274-A-G

http://identifiers.org/hco/10/GRCh38#12081688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#5937146-C-A

12081688-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5937146-C-G

12081688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5937146-C-T

12081689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5937145-T-C

http://identifiers.org/hco/10/GRCh38#12081693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#5937141-C-A

12081693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5937141-C-T

http://identifiers.org/hco/10/GRCh38#12081701-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#5937133-A-C

12081724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5937112-G-T

12081884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5936885-G-A

12081989-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5936767-T-A

12081989-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5936767-T-G

12082098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5936670-G-A

12082106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5936662-A-G

12082121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5936647-T-C

12082262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5936444-A-G

12082333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5936376-G-A

12082333-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5936376-G-C

12082333-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5936376-G-T

12082383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5936312-T-C

12084527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5935808-T-C

12084566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 5935769-G-A

12084566-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 5935769-G-C

12087071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5935071-C-T

12087309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5934859-C-T

12087384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5934790-T-C

12087384-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5934790-T-G

12087395-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5934779-C-G

http://identifiers.org/hco/10/GRCh38#12087402-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#5934771-A-C

12087402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5934771-A-G

12087402-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5934771-A-T

12087444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5934725-G-A

12087444-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5934725-G-T

http://identifiers.org/hco/10/GRCh38#12087463-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#5934707-C-A

12087463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5934707-C-T

http://identifiers.org/hco/10/GRCh38#12087502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#5934668-C-A

12087502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5934668-C-T

http://identifiers.org/hco/10/GRCh38#12087509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#5934661-C-A

http://identifiers.org/hco/10/GRCh38#12087511-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#5934659-C-A

12087511-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5934659-C-G

12087529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 5934647-C-T

12087646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5934530-A-G

12087685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5934491-G-A

12087685-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5934491-G-C

12087703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5934473-A-G

12087738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5934438-A-G

12089085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 5928848-T-C

http://identifiers.org/hco/10/GRCh38#12089172-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#5928761-C-A

12089172-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 5928761-C-G

12089172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 5928761-C-T

12089217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 5928716-A-G

12089278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5928659-A-G

12089330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5928613-G-A

12089330-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5928613-G-T

12091456-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5926685-T-G

12091487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5926664-C-T

12091534-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 5926624-T-A

12091534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 5926624-T-C

http://identifiers.org/hco/10/GRCh38#12091540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#5926618-C-A

12091594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 5926564-G-A

12092327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5925488-G-A

12092471-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5925324-T-G

12092477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5925318-A-G

12093896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5924611-C-T

12093928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5924579-T-C

12093933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5924574-T-C

http://identifiers.org/hco/10/GRCh38#12093983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#5924546-C-A

12093983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5924546-C-T

12094005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5924523-G-A

12094040-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5924488-T-A

12094040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5924488-T-C

12094068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 5924452-T-C

12094228-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5924292-G-C

12094276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 5924244-A-G

12094277-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 5924243-A-T

http://identifiers.org/hco/10/GRCh38#12097623-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#5922852-C-A

http://identifiers.org/hco/10/GRCh38#12097628-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#5922842-C-A

12097652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5922828-A-G

http://identifiers.org/hco/10/GRCh38#12097653-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#5922827-C-A

12097653-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5922827-C-G

12097817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5922661-T-C

12097817-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5922661-T-G

http://identifiers.org/hco/10/GRCh38#12097877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#5922601-C-A

12098010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5922321-A-G

12098011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5922320-A-G

12098013-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5922318-T-A

12098019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5922301-G-A

12098019-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5922301-G-C

12098038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5922245-G-A

12098038-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5922245-G-C

12098038-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5922245-G-T

http://identifiers.org/hco/10/GRCh38#12098039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#5922244-C-A

12098048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5922235-G-A

12098049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5922234-G-A

12098049-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5922234-G-C

12098049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5922234-G-T

12098088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5922194-T-C

12098130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5922149-A-G

http://identifiers.org/hco/10/GRCh38#12098133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#5922146-C-A

12098133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5922146-C-T

12098143-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5922135-T-G

12098147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5922131-G-A

12100206-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: missense variant
orthologous variants: 5919675-T-A

12100350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5919565-T-C

12100389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5919529-T-C

12100463-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5919468-C-G

12100465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5919466-A-G

12100503-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5919406-T-A

12100531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5919379-A-G

12100531-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5919379-A-T

12100540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5919370-G-A

12100556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5919354-C-T

12100571-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5919293-A-T

12100896-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5918934-G-T

12100913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5918884-T-C

12100973-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5918753-T-A

http://identifiers.org/hco/10/GRCh38#12100985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#5918662-C-A

12101026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5918483-T-C

12101140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: missense variant
orthologous variants: 5918362-C-T

12101217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5918276-G-A

http://identifiers.org/hco/10/GRCh38#12101222-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#5918271-C-A

12101222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5918271-C-T

12101263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5918118-G-A

12101275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5918106-G-A

12101275-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5918106-G-T

12101302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5918078-G-A

12101302-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5918078-G-T

12101403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5917967-T-C

12101545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5917828-T-C

12101560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5917813-C-T

12102294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5917396-T-C

12102304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5917386-G-A

12102304-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5917386-G-C

12102618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5917116-A-G

12106069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5917039-T-C

http://identifiers.org/hco/10/GRCh38#12106156-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#5916904-C-A

12106156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5916904-C-T

http://identifiers.org/hco/10/GRCh38#12106157-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#5916903-C-A

12106157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5916903-C-T

12106163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5916897-A-G

http://identifiers.org/hco/10/GRCh38#12106183-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#5916875-C-A

12106183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5916875-C-T

12106231-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5916788-C-G

12106231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5916788-C-T

12106314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 5916705-A-G

12106439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5916598-C-T

12106443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5916594-G-A

12106481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5916579-A-G

12106501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5916559-G-A

12106501-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5916559-G-T

http://identifiers.org/hco/10/GRCh38#12106506-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#5916554-C-A

12106506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5916554-C-T

12106527-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5916531-G-T

12106539-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5916519-T-A

12106539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5916519-T-C

http://identifiers.org/hco/10/GRCh38#12106558-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#5916498-A-C

12106610-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5916439-G-C

12107107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5915852-C-T

12107126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5915834-A-G

12107186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5915765-C-T

12107405-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5915593-T-A

12107637-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5915452-C-G

12107684-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5915404-C-G

12107738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5915381-T-C

12107758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5915359-G-A

12107758-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5915359-G-C

12107758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5915359-G-T

12107785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5915332-A-G

12107895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5915231-T-C

12108119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5914994-A-G

12112734-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5909089-C-G

12112757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5909072-G-A

12112757-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5909072-G-T

12112780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5909044-G-A

12112780-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5909044-G-C

12112780-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5909044-G-T

http://identifiers.org/hco/10/GRCh38#12112812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#5909017-C-A

12112812-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5909017-C-G

12112812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5909017-C-T

http://identifiers.org/hco/10/GRCh38#12112887-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#5908943-A-C

12112887-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5908943-A-T

12112892-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 5908938-T-A

12112984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 5908849-C-T

http://identifiers.org/hco/10/GRCh38#12113088-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#5908754-C-A

12113088-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5908754-C-G

12113088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5908754-C-T

12117606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5907927-C-T

12117626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5907907-A-G

12117652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5907880-G-A

12117653-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5907879-T-A

12117653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5907879-T-C

12117700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: missense variant
orthologous variants: 5907832-G-A

http://identifiers.org/hco/10/GRCh38#12117740-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#5907792-C-A

12117770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5907761-T-C

12117820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron variant
orthologous variants: 5907712-A-G

12118925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 5907132-G-A

12118925-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 5907132-G-T

http://identifiers.org/hco/10/GRCh38#12118975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#5907090-C-A

http://identifiers.org/hco/10/GRCh38#12120220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#5904767-C-A

12120220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5904767-C-T

http://identifiers.org/hco/10/GRCh38#12120331-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#5904666-C-A

12120331-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5904666-C-G

12120331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5904666-C-T

12120343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5904654-T-C

12120794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: missense variant
orthologous variants: 5903614-T-C

12120817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: missense variant
orthologous variants: 5903591-G-A

12121303-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: 3 prime UTR variant
orthologous variants: 5903447-G-C

12121304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: 3 prime UTR variant
orthologous variants: 5903446-T-C

12121304-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: 3 prime UTR variant
orthologous variants: 5903446-T-G

12121834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: 3 prime UTR variant
orthologous variants: 5903269-G-A

12121834-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: 3 prime UTR variant
orthologous variants: 5903269-G-T

12121841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: 3 prime UTR variant
orthologous variants: 5903262-T-C

12121909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: 3 prime UTR variant
orthologous variants: 5903188-A-G

http://identifiers.org/hco/10/GRCh38#12122290-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#5902213-C-A

12122290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: 3 prime UTR variant
orthologous variants: 5902213-C-T

12122349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 5902768-G-A

12122349-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 5902768-G-T

12122372-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 5902747-T-G

12122430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 5902694-A-G

http://identifiers.org/hco/10/GRCh38#12122433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#5902667-C-A

12122438-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 5902662-T-A

12122438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 5902662-T-C

http://identifiers.org/hco/10/GRCh38#12122449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#5902651-C-A

12122467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: 3 prime UTR variant
orthologous variants: 5902637-A-G

12122669-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 5902177-C-G

12122670-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 5902176-T-G

12122765-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 5902108-G-T

12122809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 5902066-T-C

12122837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 5902037-T-C

12122837-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 5902037-T-G

http://identifiers.org/hco/10/GRCh38#12122843-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#5902031-C-A

12122845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 5902029-T-C

12122881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 5901994-G-A

12122881-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 5901994-G-C

12122881-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 5901994-G-T

12122883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 5901992-G-A

http://identifiers.org/hco/10/GRCh38#12122896-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#5901980-C-A

http://identifiers.org/hco/10/GRCh38#12122902-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#5901974-C-A

http://identifiers.org/hco/10/GRCh38#12122921-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#5901955-C-A

12122921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 5901955-C-T

12122925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23537
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 5901951-T-C