127118706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29411801-G-A

127118749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29411759-G-A

http://identifiers.org/hco/6/GRCh38#127118800-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#29411711-C-A

127118800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29411711-C-T

127118832-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29411679-C-G

127118832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29411679-C-T

127118964-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29411566-C-G

127118964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29411566-C-T

127119167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29411348-A-G

127119304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29411211-T-C

127119322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29411109-T-C

127119361-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29411070-G-T

127119371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29411060-C-T

http://identifiers.org/hco/6/GRCh38#127119381-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#29411050-C-A

127119381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29411050-C-T

http://identifiers.org/hco/6/GRCh38#127119385-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#29411046-C-A

127119385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29411046-C-T

127119565-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29410889-T-C

127119683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29410782-A-G

127119816-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29410650-G-C

http://identifiers.org/hco/6/GRCh38#127119886-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#29410585-C-A

127119886-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29410585-C-G

127119886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29410585-C-T

127119904-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29410571-G-T

http://identifiers.org/hco/6/GRCh38#127119921-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#29410554-C-A

127119928-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29410547-A-T

http://identifiers.org/hco/6/GRCh38#127120054-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#29410425-C-A

127120054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29410425-C-T

127120055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29410424-G-A

127120055-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29410424-G-T

127120085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29410397-G-A

127120085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29410397-G-T

127120479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29410033-G-A

127120507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29410005-C-T

127120946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 29409577-G-T

http://identifiers.org/hco/6/GRCh38#127121262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#29409267-C-A

127121262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29409267-C-T

127121272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29409257-G-A

127121272-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29409257-G-C

127121720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29408839-C-T

127121761-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29408810-G-T

127121826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29408761-G-A

127121826-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29408761-G-C

127122093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29408477-T-C

127122212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29408398-T-C

127122324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29408291-T-C

127122325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29408290-G-A

127122325-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29408290-G-T

127122641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29407803-T-C

http://identifiers.org/hco/6/GRCh38#127122734-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#29407710-C-A

127122734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29407710-C-T

127122845-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29407610-A-T

127122892-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29407565-T-A

127123001-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29407453-A-T

127123191-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29407308-G-C

127123426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29407095-A-G

127124158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29406406-T-C

127124236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29406336-T-C

127124733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29405841-A-G

127124764-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29405804-G-C

127124833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29405737-T-C

127125026-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29405544-T-G

127125781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29405331-A-G

http://identifiers.org/hco/6/GRCh38#127125850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#29405261-C-A

127126257-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29404867-T-A

127126534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29404604-A-G

http://identifiers.org/hco/6/GRCh38#127126728-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#29404417-A-C

127126733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29404411-A-G

127126818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29404351-A-G

127127124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29404065-C-T

127127137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29404052-C-T

127127343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29403883-C-T

127127736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29403510-G-A

127127736-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29403510-G-C

127127739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29403507-G-A

127127815-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29403485-T-G

127127843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29403458-A-G

127128117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29403216-T-C

127128175-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29403158-G-C

http://identifiers.org/hco/6/GRCh38#127128777-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#29402626-A-C

127128779-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29402624-G-C

127128838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29402565-T-C

http://identifiers.org/hco/6/GRCh38#127128892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#29402533-C-A

127128956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29402472-T-C

http://identifiers.org/hco/6/GRCh38#127129175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#29402237-C-A

127129175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29402237-C-T

http://identifiers.org/hco/6/GRCh38#127129176-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#29402236-A-C

127129385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29402033-C-T

127129555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29401864-A-G

127129679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29401741-C-T

127129711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29401702-T-C

127129712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29401701-G-A

127129838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29401589-A-G

http://identifiers.org/hco/6/GRCh38#127130000-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#29401423-A-C

127130247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29401174-C-T

127130305-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29401123-T-A

127130343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29401074-G-A

127130343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29401074-G-T

127130354-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29401062-G-T

127131783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29400447-T-C

127131849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29400376-G-A

127131849-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29400376-G-T

127131867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29400358-A-G

127132416-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29399823-G-C

127132491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29399750-G-A

127132512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29399731-G-A

127132512-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29399731-G-T

127132618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29399631-G-A

http://identifiers.org/hco/6/GRCh38#127132726-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#29399525-A-C

http://identifiers.org/hco/6/GRCh38#127132749-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#29399505-C-A

http://identifiers.org/hco/6/GRCh38#127133050-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#29398904-C-A

127133152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29398762-A-G

127133621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29398302-G-A

127133730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29398212-A-G

127133741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29398201-G-A

127133741-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29398201-G-T

127133979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29397960-T-C

127133993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29397946-C-T

127134022-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29397916-A-T

127134639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29397311-C-T

127134650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29397300-A-G

127134794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29397163-A-G

127134847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29397129-G-A

127134940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29397058-G-A

127134940-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29397058-G-C

http://identifiers.org/hco/6/GRCh38#127135486-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#29396824-A-C

127135486-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29396824-A-T

127137604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29395723-A-G

127137631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29395696-T-C

http://identifiers.org/hco/6/GRCh38#127137888-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#29395465-A-C

127137969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29395385-T-C

127138026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29395336-A-G

127138031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29395331-T-C

127138277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29394964-T-C

127138682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29392505-G-A

127138864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29392325-A-G

127138993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29392196-A-G

127139005-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29392187-A-T

127140015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29391332-A-G

127140073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29391271-G-A

127140691-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29390699-G-C

http://identifiers.org/hco/6/GRCh38#127140720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#29390670-C-A

127140796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29390594-A-G

http://identifiers.org/hco/6/GRCh38#127141037-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#29390372-C-A

127141126-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29390286-C-G

http://identifiers.org/hco/6/GRCh38#127142231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#29389478-C-A

http://identifiers.org/hco/6/GRCh38#127142247-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#29389462-C-A

127142260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29389449-T-C

127142513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29389223-C-T

127143579-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29388690-G-T

127143671-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29388634-T-A

127143688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29388617-C-T

127143803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29388513-G-A

127143805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29388511-C-T

127143925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29388379-T-C

127145034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29387110-T-C

127145078-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29387087-T-G

127145450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29386006-G-A

127145595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29385868-C-T

127145702-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29385762-G-C

127146418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29385078-A-G

127146996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29384532-G-A

127147307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29384225-A-G

127147324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29383937-C-T

127147514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29383761-T-C

127147528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29383747-C-T

127147543-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29383732-T-G

127147545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29383730-A-G

127147567-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29383708-G-C

127147673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29383626-G-A

http://identifiers.org/hco/6/GRCh38#127147692-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#29383607-C-A

127147827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29383504-T-C

127147827-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29383504-T-G

127147860-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29383463-A-T

127147991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29383372-G-A

127148121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29383246-C-T

127148254-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29383100-G-T

127148327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29382910-T-C

http://identifiers.org/hco/6/GRCh38#127148490-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#29382734-A-C

127148507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29382717-T-C

http://identifiers.org/hco/6/GRCh38#127148522-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#29382702-C-A

127148522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29382702-C-T

http://identifiers.org/hco/6/GRCh38#127148527-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#29382697-C-A

http://identifiers.org/hco/6/GRCh38#127148541-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#29382683-C-A

127148541-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29382683-C-G

127148541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29382683-C-T

127148548-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29382676-T-A

127148548-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29382676-T-C

127148641-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 29382580-T-G

http://identifiers.org/hco/6/GRCh38#127148870-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#29382344-C-A

127148879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29382335-G-A

127148879-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29382335-G-C

127148879-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29382335-G-T

127148898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29382316-A-G

127148898-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29382316-A-T

127148923-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29382291-T-A

127148923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29382291-T-C

127148946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29382274-G-T

http://identifiers.org/hco/6/GRCh38#127149195-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#29382016-A-C

127149603-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29381660-C-G

127149728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29381535-G-A

http://identifiers.org/hco/6/GRCh38#127149770-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#29381503-A-C

127149778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29381495-T-C

127149781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29381492-A-G

127149826-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29381447-A-T

127149939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29381340-G-A

127150168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29381068-T-C

127150168-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29381068-T-G

127150213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29380956-G-A

127150230-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29380906-T-A

127150253-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29380883-C-G

127150253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29380883-C-T

127150292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29380844-T-C

127150292-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29380844-T-G

127150306-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29380830-T-G

127150385-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29380766-G-T

127150677-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29380491-T-A

127150677-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29380491-T-G

http://identifiers.org/hco/6/GRCh38#127150678-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#29380490-C-A

127150678-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29380490-C-G

127150984-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29380254-G-C

127151416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29379912-G-A

127151525-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29379806-G-T

127151765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29379572-T-C

127151833-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29379510-C-G

127151861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29379490-G-A

127151922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29379429-T-C

http://identifiers.org/hco/6/GRCh38#127151927-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#29379424-A-C

127152017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29379347-A-G

127152057-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29379317-T-A

http://identifiers.org/hco/6/GRCh38#127152282-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#29379117-C-A

127152391-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29379018-G-C

127152686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29378758-T-C

127152787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29378667-G-A

127152787-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29378667-G-C

http://identifiers.org/hco/6/GRCh38#127152837-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#29378618-A-C

127152901-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29378566-A-G

127152924-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29378543-A-T

http://identifiers.org/hco/6/GRCh38#127153029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#29378439-C-A

127153029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29378439-C-T

127153033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29378435-T-C

127153698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29377818-G-T

127154311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29377178-A-G

127154311-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29377178-A-T

127154329-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29377157-C-G

127154929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29376383-T-C

127154955-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29376357-C-G

127155029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29376304-G-A

127155061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29376274-A-G

127155097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29376255-T-C

127155100-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29376252-T-G

127155104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29376248-G-A

127155104-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29376248-G-T

127155142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29376209-A-G

127155149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29376207-G-A

127155149-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29376207-G-C

127155149-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29376207-G-T

http://identifiers.org/hco/6/GRCh38#127155156-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#29376199-C-A

127155156-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29376199-C-G

127155162-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29376193-G-C

127155198-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29376180-T-G

127155206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29376172-A-G

127155215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29376164-A-G

127155279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29376085-T-C

127155297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 29376067-A-G

http://identifiers.org/hco/6/GRCh38#127155478-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#29375886-A-C

127155478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29375886-A-G

127155527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29375837-T-C

http://identifiers.org/hco/6/GRCh38#127155532-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#29375832-C-A

127156243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29375413-G-A

127156734-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29374944-C-G

127156747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29374931-G-T

http://identifiers.org/hco/6/GRCh38#127157385-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#29374326-C-A

127157537-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29374190-A-T

127157812-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29373920-G-T

127157921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29373737-T-C

127157931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29373727-T-C

127157969-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29373685-C-G

127158022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29373633-T-C

127158522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29373145-G-A

http://identifiers.org/hco/6/GRCh38#127161945-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#29372734-A-C

http://identifiers.org/hco/6/GRCh38#127162665-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#29370610-C-A

127162670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29370605-C-T

127162713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29370554-G-A

127162928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29370339-T-C

127163010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29370256-C-T

127163967-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29369349-C-G

http://identifiers.org/hco/6/GRCh38#127164106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#29369223-C-A

127164106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29369223-C-T

http://identifiers.org/hco/6/GRCh38#127164183-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#29369133-A-C

127164334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29369000-C-T

127164375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29368957-T-C

127164483-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29368840-T-G

127164533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29368789-A-G

127164657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29368682-T-C

127164672-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29368667-C-G

127164717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29368622-T-C

127164787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29368552-T-C

127165121-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29368137-A-T

127165222-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29367877-G-T

http://identifiers.org/hco/6/GRCh38#127165274-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#29367815-A-C

127165554-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29367547-T-A

127170510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29363800-A-G

127170645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29363666-T-C

127170662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29363649-T-C

127170869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29363444-G-A

127170869-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29363444-G-T

127171360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29362766-G-A

127171360-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29362766-G-C

127171391-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29362733-A-T

127171431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29362694-G-A

127171609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29362519-G-A

127171696-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29362448-G-T

127172044-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29362105-G-C

http://identifiers.org/hco/6/GRCh38#127172222-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#29361932-A-C

127172464-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29361695-A-T

http://identifiers.org/hco/6/GRCh38#127172548-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#29361609-A-C

http://identifiers.org/hco/6/GRCh38#127172624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#29361539-C-A

127173600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29360719-G-A

http://identifiers.org/hco/6/GRCh38#127173646-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#29360670-C-A

127173772-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29360544-G-C

127173969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29360358-C-T

127174325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29359200-A-G

http://identifiers.org/hco/6/GRCh38#127174339-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#29359186-A-C

127174527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29359017-G-A

127174527-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29359017-G-T

127176641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29356847-C-T

127176984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29356527-T-C

127177654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29356010-G-A

127178755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29355643-T-C

127178813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29355585-G-T

127178858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29355539-T-C

127178888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29355509-G-A

127178933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29355480-A-G

127179269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29355226-G-A

127179424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29355070-G-A

127179780-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29354685-G-C

127180372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29353158-G-A

127180420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29353118-A-G

127180463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29353075-A-G

http://identifiers.org/hco/6/GRCh38#127180476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#29353059-C-A

http://identifiers.org/hco/6/GRCh38#127180502-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#29352905-A-C

http://identifiers.org/hco/6/GRCh38#127180508-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#29352892-A-C

127180528-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29352852-T-A

127180547-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29352825-G-T

127180628-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29352640-G-T

127180937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29352358-G-A

127181002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29352293-T-C

http://identifiers.org/hco/6/GRCh38#127181132-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#29352164-A-C

127181183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29352116-C-T

127181288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29351960-G-A

127181305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29351943-C-T

127181342-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29351888-A-T

127181422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29351802-T-C

127181720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29351523-T-C

127182576-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29350865-T-G

http://identifiers.org/hco/6/GRCh38#127182628-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#29350811-A-C

127182635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29350001-T-C

127182660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29349976-C-T

127184207-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29348875-C-G

127184370-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29348729-T-A

127184391-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29348711-G-T

127184600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29348522-T-C

127184884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29348118-G-A

127184884-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29348118-G-C

127184998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29348020-C-T

http://identifiers.org/hco/6/GRCh38#127185304-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#29347773-C-A

127185504-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29346969-T-A

127185615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29346865-C-T

127185849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29346672-C-T

127185945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29346578-T-C

127186386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29346101-G-A

127186386-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29346101-G-C

127186817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29345472-G-T

127187516-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29343824-A-T

http://identifiers.org/hco/6/GRCh38#127187566-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#29343774-C-A

127187599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29343741-A-G

127187682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29343659-T-C

127187828-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29343517-T-G

127187978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29343365-T-C

127187999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29343344-T-C

127189269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29337110-G-A

127189315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29337056-G-A

http://identifiers.org/hco/6/GRCh38#127189387-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#29336988-A-C

127190605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29335997-A-G

127190940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29335675-T-C

127190950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29335665-A-G

http://identifiers.org/hco/6/GRCh38#127191078-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#29335513-C-A

127191089-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29335502-G-T

127191101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29335490-T-C

127191273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29335329-T-C

http://identifiers.org/hco/6/GRCh38#127191662-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#29334504-A-C

127191798-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29334272-G-T

127191950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29334131-G-A

127192439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29333687-A-G

127192461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29333665-C-T

127192500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29333627-T-C

127192514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29333613-A-G

127192514-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29333613-A-T

127192615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29333127-T-C

127192623-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29333119-T-G

127192661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 29333079-G-A

127192661-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 29333079-G-C

http://identifiers.org/hco/6/GRCh38#127192738-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#29333002-C-A

127192738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29333002-C-T

http://identifiers.org/hco/6/GRCh38#127192754-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#29332986-A-C

127192792-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29332950-G-C

127193092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29332631-G-A

127193229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29332489-C-T

127193298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29332420-C-T

127193417-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29332300-G-T

127193721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29332002-C-T

http://identifiers.org/hco/6/GRCh38#127193784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#29331918-C-A

127193928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29331787-G-A

127193968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29331732-A-G

http://identifiers.org/hco/6/GRCh38#127194130-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#29331578-C-A

127194309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29331397-T-C

http://identifiers.org/hco/6/GRCh38#127194556-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#29331168-C-A

http://identifiers.org/hco/6/GRCh38#127194586-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#29331136-C-A

http://identifiers.org/hco/6/GRCh38#127194940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#29330817-C-A

127194940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29330817-C-T

127195706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29330436-T-C

http://identifiers.org/hco/6/GRCh38#127195717-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#29330425-C-A

http://identifiers.org/hco/6/GRCh38#127195911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#29330229-C-A

127195911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 29330229-C-T

http://identifiers.org/hco/6/GRCh38#127196057-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#29330074-A-C

127196342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29329783-T-C

127196498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29329628-G-A

127196498-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29329628-G-T

http://identifiers.org/hco/6/GRCh38#127196594-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#29329542-C-A

127196594-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29329542-C-G

127196778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29329360-T-C

127196830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29329308-A-G

http://identifiers.org/hco/6/GRCh38#127197192-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#29328972-A-C

http://identifiers.org/hco/6/GRCh38#127197198-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#29328966-C-A

127197198-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29328966-C-G

127197198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29328966-C-T

127197284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29328880-G-A

127197284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29328880-G-T

127197382-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29328791-T-G

127197386-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29328787-T-G

127197412-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29328759-G-C

127197412-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29328759-G-T

127197413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29328758-T-C

http://identifiers.org/hco/6/GRCh38#127197568-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#29328605-A-C

127197579-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29328594-G-T

127198355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29327904-C-T

http://identifiers.org/hco/6/GRCh38#127198412-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#29327848-C-A

127198450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29327813-T-C

127198548-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29327765-A-T

127199332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29327562-C-T

127199357-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29327533-T-A

127199443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20866
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29327454-A-G