http://identifiers.org/hco/13/GRCh38#100603998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123156454-C-A

http://identifiers.org/hco/13/GRCh38#100604201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123156667-C-A

http://identifiers.org/hco/13/GRCh38#100604233-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123156699-C-A

100604528-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 123156977-A-T

100604544-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 123156993-C-G

100604719-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 123157130-T-G

http://identifiers.org/hco/13/GRCh38#100604927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123157345-C-A

100604927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 123157345-C-T

100605209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123157622-T-C

100605275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123157676-G-A

100605275-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123157676-G-T

http://identifiers.org/hco/13/GRCh38#100605325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123157729-C-A

http://identifiers.org/hco/13/GRCh38#100606447-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123158734-A-C

http://identifiers.org/hco/13/GRCh38#100606467-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123158750-A-C

100606525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123158787-C-T

100606703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123158955-T-C

100606847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123159113-C-T

100606897-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123159165-T-A

100606897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123159165-T-C

100607138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123159395-C-T

http://identifiers.org/hco/13/GRCh38#100607737-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123159647-C-A

100607784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123159680-T-C

100607878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123159767-G-A

100609365-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123160703-G-T

100609417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123160756-T-C

100609607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123160894-T-C

100609785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123161034-G-A

100609855-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123161102-T-G

100609856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123161103-G-A

100609872-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123161115-G-C

100609883-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123161126-T-G

100609974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123161202-G-A

100610048-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123161295-G-T

100610051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123161298-A-G

100610263-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123161563-C-G

100610360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123161640-T-C

100610519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123161817-G-A

http://identifiers.org/hco/13/GRCh38#100611135-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123162391-A-C

100612205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123163213-A-G

http://identifiers.org/hco/13/GRCh38#100612303-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123163287-C-A

100612303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123163287-C-T

100612425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123163403-G-A

100612545-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123163511-T-G

100612587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123163547-G-A

100612587-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123163547-G-C

100612587-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123163547-G-T

100612799-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123163704-T-G

100613499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123164122-T-C

http://identifiers.org/hco/13/GRCh38#100614543-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123165187-A-C

100614701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123165313-A-G

100614702-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123165314-G-C

100614800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123165416-G-A

100614800-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123165416-G-T

http://identifiers.org/hco/13/GRCh38#100614848-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123165449-A-C

100614848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123165449-A-G

http://identifiers.org/hco/13/GRCh38#100619648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123166724-C-A

100619648-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123166724-C-G

100619756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123166837-T-C

100620020-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123167056-G-C

100620355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123167290-G-A

100620456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123167352-T-C

100620796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123167730-C-T

http://identifiers.org/hco/13/GRCh38#100620811-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123167745-C-A

100620895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123167808-T-C

100621006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123167914-A-G

100621110-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123167987-A-T

100621112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123167989-A-G

100621132-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123168000-G-C

100621188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123168055-C-T

100621215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123168082-C-T

100621881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123168376-C-T

100622324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123168934-T-C

100622932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123169093-C-T

100622933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123169094-G-A

100623019-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123169178-G-T

100623042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123169202-A-G

100624981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123169711-A-G

100625007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123169735-G-A

100625007-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123169735-G-T

100625072-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123169798-T-A

http://identifiers.org/hco/13/GRCh38#100625140-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123169866-A-C

100625140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123169866-A-G

100625140-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123169866-A-T

100625330-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123170052-A-T

100625343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123170065-G-T

100625367-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123170089-A-T

100625384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123170104-G-A

100625384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123170104-G-T

100625424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123170143-A-G

100625522-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123170219-A-T

100625646-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123170343-T-G

100625658-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123170355-C-G

100625658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123170355-C-T

100625728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123170437-C-T

100625771-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123170495-A-T

100626033-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123170721-T-G

100628566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123172418-T-C

100628787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123172622-G-A

100629426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123173156-C-T

100629622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123173330-T-C

100630580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123173872-C-T

100630664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123173954-G-A

100630664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123173954-G-T

100630813-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123174097-C-G

100631754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123174990-T-C

100632469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123175590-C-T

100632515-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123175631-A-T

100634330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123178291-G-A

http://identifiers.org/hco/13/GRCh38#100634651-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123178573-C-A

100634696-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123178600-T-A

100634696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123178600-T-C

100634696-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123178600-T-G

100634717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123178654-T-C

http://identifiers.org/hco/13/GRCh38#100634745-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123178682-C-A

100634745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123178682-C-T

100634868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123178780-G-A

100635206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123179409-A-G

100635224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123179428-G-A

100635224-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123179428-G-T

http://identifiers.org/hco/13/GRCh38#100635695-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123179776-C-A

100635695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123179776-C-T

100635721-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123179784-G-T

100635722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123179785-A-G

100635779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 123179835-C-T

100635805-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123179861-A-T

http://identifiers.org/hco/13/GRCh38#100635889-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123179946-A-C

100635889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123179946-A-G

100635889-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123179946-A-T

100636098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123180177-A-G

http://identifiers.org/hco/13/GRCh38#100636164-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123180232-A-C

http://identifiers.org/hco/13/GRCh38#100636165-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123180233-C-A

100636165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123180233-C-T

100636499-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123180534-G-C

100636600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123180635-T-C

100636845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123180876-A-G

100636991-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123181027-C-G

100636991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123181027-C-T

100637619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123182167-G-A

100637640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123182188-C-T

100637897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123182887-A-G

100637944-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 123182934-C-G

100637944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 123182934-C-T

100638206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123183181-G-A

100638206-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123183181-G-C

100638206-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123183181-G-T

http://identifiers.org/hco/13/GRCh38#100638235-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123183212-C-A

100638298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123183273-A-G

100638315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123183290-A-G

100638389-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123183346-G-C

100638389-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123183346-G-T

100638404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123183365-G-A

100638404-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123183365-G-C

100638404-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123183365-G-T

100638416-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123183379-G-T

http://identifiers.org/hco/13/GRCh38#100638438-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123183401-C-A

100638457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123183420-A-G

100638475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123183431-A-G

100638531-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123183488-G-T

http://identifiers.org/hco/13/GRCh38#100638540-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123183495-A-C

http://identifiers.org/hco/13/GRCh38#100638634-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123183606-C-A

100638634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123183606-C-T

100638635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123183607-G-A

100638635-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123183607-G-T

100638825-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 123183774-G-T

100638826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 123183775-A-G

100638909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123183861-T-C

http://identifiers.org/hco/13/GRCh38#100638933-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123183885-C-A

100638933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123183885-C-T

100640507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123185267-G-A

http://identifiers.org/hco/13/GRCh38#100642141-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123187561-C-A

100642141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123187561-C-T

100642343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123188027-G-A

100642423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123188107-A-G

100642482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123188183-T-C

100642621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123188296-C-T

100642645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123188319-C-T

100642692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123188362-T-C

100642734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123188418-G-A

100643026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123188663-A-G

100643521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123189072-C-T

100645705-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123190175-T-G

100645711-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123190181-G-C

100646015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123190410-A-G

100646241-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123190818-G-C

100647492-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123191627-G-C

100647670-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123191794-G-T

100647763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123191879-C-T

100647767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123191883-A-G

http://identifiers.org/hco/13/GRCh38#100648069-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123193196-A-C

100648250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123193364-G-A

http://identifiers.org/hco/13/GRCh38#100648605-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123193895-A-C

100649523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123194669-T-C

100649523-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123194669-T-G

100649633-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123194752-A-T

100649637-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123194756-C-G

100649637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123194756-C-T

100649730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123194848-G-A

http://identifiers.org/hco/13/GRCh38#100649772-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123194889-A-C

100649807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123194915-A-G

100650307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123195352-G-A

100650597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123195639-G-A

100650609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123195651-C-T

100650812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123195963-C-T

100650898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123196070-T-C

100651178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123196527-T-C

100651196-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123196555-G-T

100651252-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123196611-A-T

100651274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123196633-T-C

100651319-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123196679-G-C

100651327-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123196687-C-G

100651469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123196797-A-G

100651489-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123196816-T-A

100651491-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123196818-T-A

100651491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123196818-T-C

http://identifiers.org/hco/13/GRCh38#100651531-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123196865-C-A

100651559-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123196895-A-T

http://identifiers.org/hco/13/GRCh38#100651564-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123196900-C-A

100651564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123196900-C-T

http://identifiers.org/hco/13/GRCh38#100651570-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123196906-A-C

100651946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123197329-A-G

100652960-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123197946-A-T

100652981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123197967-T-C

100653034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123198026-G-A

100653160-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123198139-G-C

100653166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123198142-G-A

100653189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123198165-T-C

100653251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123198226-T-C

100653486-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123198400-G-T

100653681-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123198522-G-T

100653846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123198631-C-T

100653895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123198681-T-C

100654154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123198878-C-T

100654221-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123198936-A-G

100654235-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123198950-G-C

100654241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123198956-G-A

100654251-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123198967-C-G

100654274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123198990-T-C

http://identifiers.org/hco/13/GRCh38#100654358-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123199073-A-C

100654358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123199073-A-G

100654618-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123199406-T-A

100654654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123199437-A-G

http://identifiers.org/hco/13/GRCh38#100654656-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123199438-A-C

100654718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123199508-A-G

100654722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123199512-G-A

100654722-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123199512-G-C

100654778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123199569-C-T

100654811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123199601-C-T

100654884-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123199676-C-G

100654901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123199693-C-T

100655398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123199842-G-A

100655528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123199947-T-C

100655996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123200366-C-T

100656148-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123200515-A-T

100656229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123200566-A-G

100656273-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123200603-G-T

http://identifiers.org/hco/13/GRCh38#100656283-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123200612-C-A

100656283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123200612-C-T

100656310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123200639-G-A

100656310-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123200639-G-T

100656340-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123200669-T-A

100656340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123200669-T-C

100656370-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123200699-A-T

http://identifiers.org/hco/13/GRCh38#100656418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123200747-C-A

100656460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123200789-A-G

http://identifiers.org/hco/13/GRCh38#100656509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123200825-C-A

100657126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123201107-C-T

100657438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123203056-C-T

http://identifiers.org/hco/13/GRCh38#100657451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123203068-C-A

100657604-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123203224-C-G

100657773-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123203318-T-A

100657798-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123203341-T-G

100657810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123203353-A-G

100658355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123204508-C-T

100658496-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123204626-C-G

100659191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123205367-G-A

100659457-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123205595-T-A

100659457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123205595-T-C

100659677-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123206289-G-C

100659976-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123206682-G-C

100660000-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123206704-A-T

100660593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123206920-G-A

http://identifiers.org/hco/13/GRCh38#100662904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123209098-C-A

100662906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123209100-T-C

100662906-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123209100-T-G

http://identifiers.org/hco/13/GRCh38#100662922-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123209109-C-A

100662922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123209109-C-T

100662923-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123209110-T-G

100662932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123209119-G-A

100662932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123209119-G-T

100662949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123209137-G-A

100662996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123209184-G-A

100663024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123209212-G-A

100663241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123209418-G-A

100663241-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123209418-G-T

100663462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123209544-T-C

100663598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123209852-T-C

100663616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123209871-C-T

http://identifiers.org/hco/13/GRCh38#100663840-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123210063-A-C

100663908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123210130-G-A

http://identifiers.org/hco/13/GRCh38#100664216-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123210577-C-A

100664216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123210577-C-T

100664298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123210659-A-G

100664393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123210825-A-G

100664465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123210897-G-A

100664490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123210911-C-T

100664609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123211003-T-C

100664950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123211414-C-T

100665327-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123211740-G-T

100666017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 123212389-G-A

100666018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 123212390-G-A

100666018-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 123212390-G-T

100666026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 123212398-T-C

http://identifiers.org/hco/13/GRCh38#100666230-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123212584-C-A

100666562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123212899-A-G

100666565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123212902-G-A

100666571-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123212908-G-C

100666663-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123212963-G-T

100667088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123214015-C-T

100667344-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123214211-G-C

100667428-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123214294-C-G

100667428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123214294-C-T

100667523-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123214327-T-A

100667523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123214327-T-C

100667523-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123214327-T-G

100667809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123214828-C-T

http://identifiers.org/hco/13/GRCh38#100668073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123215039-C-A

100668275-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123215228-G-C

100668275-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123215228-G-T

100668429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123215336-T-C

100668431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123215338-T-C

100668545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123215455-G-A

100668836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123215730-G-A

100668836-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123215730-G-T

100668855-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123215749-G-T

100668906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123215811-T-C

100669052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123215951-A-G

100669213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123216104-G-A

100669648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123216450-C-T

100669735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123216527-C-T

100670104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123217070-T-C

100670173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123217139-G-A

100670173-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123217139-G-T

100670251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123217207-G-T

100670265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123217218-G-A

100670265-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123217218-G-C

100670265-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123217218-G-T

100670318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123217272-T-C

100670343-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123217297-C-G

100670343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123217297-C-T

http://identifiers.org/hco/13/GRCh38#100670365-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123217319-C-A

100670365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123217319-C-T

http://identifiers.org/hco/13/GRCh38#100670483-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123217426-C-A

100670483-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123217426-C-G

100670483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123217426-C-T

http://identifiers.org/hco/13/GRCh38#100670611-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123217553-A-C

100670611-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123217553-A-T

100670983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123217633-T-C

100671065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123217688-T-C

100671421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123217869-C-T

100671572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123217999-G-A

100671693-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123218114-G-C

100672164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123218503-C-T

100672259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123218568-G-A

100672861-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123218832-G-C

100672952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123218915-A-G

100673039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123219030-G-A

100673100-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123219081-G-C

100673100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123219081-G-T

100673135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123219112-C-T

100673338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123219324-A-G

100673834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123219750-C-T

100673859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123219767-A-G

100673921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123219813-G-A

http://identifiers.org/hco/13/GRCh38#100673922-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123219814-C-A

100674118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123220000-C-T

100674431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123220277-G-A

http://identifiers.org/hco/13/GRCh38#100674474-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#123220320-A-C

100674474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 123220320-A-G

100674474-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 123220320-A-T

100674533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 123220371-T-C

100674561-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 123220399-C-G

100674561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 123220399-C-T

100674581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123220420-C-T

http://identifiers.org/hco/13/GRCh38#100674608-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123220447-C-A

100674767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123220607-C-T

http://identifiers.org/hco/13/GRCh38#100674838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123220673-C-A

100674838-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 123220673-C-G

100674838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 123220673-C-T

100674843-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 123220678-G-C

100674843-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 123220678-G-T

http://identifiers.org/hco/13/GRCh38#100674850-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123220682-A-C

100674850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 123220682-A-G

http://identifiers.org/hco/13/GRCh38#100674856-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123220688-C-A

100674856-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 123220688-C-G

100674856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 123220688-C-T

100674915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: intron variant
orthologous variants: 123220746-T-C

http://identifiers.org/hco/13/GRCh38#100674982-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123220803-C-A

100674982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: 5 prime UTR variant
orthologous variants: 123220803-C-T

http://identifiers.org/hco/13/GRCh38#100674991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123220812-C-A

100674991-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: 5 prime UTR variant
orthologous variants: 123220812-C-G

100675004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 123220823-G-A

100675004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 123220823-G-T

http://identifiers.org/hco/13/GRCh38#100675021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#123220842-C-A

100675021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25904
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 123220842-C-T