52857317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45696297-C-T

http://identifiers.org/hco/14/GRCh38#52857329-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45696309-C-A

52857329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45696309-C-T

http://identifiers.org/hco/14/GRCh38#52857370-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45696351-C-A

52857451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45696430-C-T

52857453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45696432-A-G

52857550-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45696527-T-G

52857808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45696787-A-G

52857912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45696886-T-C

52857912-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45696886-T-G

52858006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45696968-G-A

52858006-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45696968-G-T

52858067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45697032-G-A

52858067-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45697032-G-C

52858067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45697032-G-T

http://identifiers.org/hco/14/GRCh38#52858087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45697050-C-A

52858087-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45697050-C-G

http://identifiers.org/hco/14/GRCh38#52858175-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45697097-A-C

http://identifiers.org/hco/14/GRCh38#52858192-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45697116-A-C

52858192-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45697116-A-T

52858270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45697199-G-T

http://identifiers.org/hco/14/GRCh38#52858584-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45697512-C-A

52858584-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45697512-C-G

52858584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45697512-C-T

52858702-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45697587-T-A

52858702-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45697587-T-G

http://identifiers.org/hco/14/GRCh38#52858735-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45697615-C-A

52858752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45697632-A-G

http://identifiers.org/hco/14/GRCh38#52858819-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45697679-C-A

52858819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45697679-C-T

http://identifiers.org/hco/14/GRCh38#52858849-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45697705-C-A

52858849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45697705-C-T

http://identifiers.org/hco/14/GRCh38#52858854-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45697710-C-A

52859007-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45698064-G-T

52859133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45698164-T-C

52859148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45698179-C-T

http://identifiers.org/hco/14/GRCh38#52859169-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45698201-C-A

52859169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45698201-C-T

52859176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45698208-G-A

52859233-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45698279-T-A

52859250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45698295-A-G

http://identifiers.org/hco/14/GRCh38#52859279-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45698326-C-A

http://identifiers.org/hco/14/GRCh38#52859315-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45698363-A-C

52859315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45698363-A-G

52859316-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45698364-G-T

52859675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 45699326-T-C

http://identifiers.org/hco/14/GRCh38#52859714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45699365-C-A

52859714-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 45699365-C-G

52859714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 45699365-C-T

52860212-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45699460-G-C

52860212-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45699460-G-T

52860228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45699476-T-C

52860228-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45699476-T-G

52860270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45699519-T-C

52860322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45699560-G-A

http://identifiers.org/hco/14/GRCh38#52860323-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45699561-A-C

52860367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 45699599-T-C

52860486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45699720-C-T

52860527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45699752-C-T

http://identifiers.org/hco/14/GRCh38#52860590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45699802-C-A

52860590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45699802-C-T

52860614-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45699828-A-T

http://identifiers.org/hco/14/GRCh38#52860617-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45699831-C-A

52860617-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45699831-C-G

52860617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45699831-C-T

http://identifiers.org/hco/14/GRCh38#52860692-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45699886-A-C

52860692-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45699886-A-T

52860718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45699917-G-A

52860718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45699917-G-T

52860965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45700122-T-C

52861003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45700161-G-A

52861003-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45700161-G-T

52861088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45700253-A-G

52861141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45700303-A-G

52861264-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45700421-C-G

52861282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45700431-T-C

52861310-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45700456-T-A

52861310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45700456-T-C

52861310-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45700456-T-G

52861365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45700506-T-C

52861465-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45700586-A-T

http://identifiers.org/hco/14/GRCh38#52863087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45701238-C-A

http://identifiers.org/hco/14/GRCh38#52863439-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45701580-C-A

52863653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45701790-T-C

52863721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45701858-T-C

52863841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45701973-G-A

52863995-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45702030-G-T

http://identifiers.org/hco/14/GRCh38#52864350-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45702138-A-C

52864350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45702138-A-G

52864350-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45702138-A-T

52864366-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45702154-C-G

52864431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 45702211-G-T

52864457-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45702237-T-A

52864457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45702237-T-C

52864458-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45702238-A-T

52864608-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 45702388-T-G

52864657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45702442-C-T

52864697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45702484-G-A

http://identifiers.org/hco/14/GRCh38#52864747-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45702541-A-C

52864747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 45702541-A-G

52864895-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45702681-T-A

52864895-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45702681-T-G

52864904-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45702690-T-A

52864918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45702703-G-A

52864918-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45702703-G-T

http://identifiers.org/hco/14/GRCh38#52864922-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45702706-C-A

52864937-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45702721-A-T

52871734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45703888-C-T

52871793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45703925-A-G

52871819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45703951-A-G

52871820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45703952-C-T

52871884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45703995-G-A

52871884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45703995-G-T

52871933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45704035-A-G

52871992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45704077-G-A

http://identifiers.org/hco/14/GRCh38#52871995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45704080-C-A

52872010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45704098-A-G

http://identifiers.org/hco/14/GRCh38#52872025-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45704111-C-A

52872042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45704129-A-G

52872068-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45704143-G-T

http://identifiers.org/hco/14/GRCh38#52872239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45704238-C-A

52872239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45704238-C-T

http://identifiers.org/hco/14/GRCh38#52872273-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45704250-C-A

http://identifiers.org/hco/14/GRCh38#52872289-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45704266-C-A

52872289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45704266-C-T

52872290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45704267-T-C

52872734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45704739-G-A

52872734-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45704739-G-T

52872782-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45704778-T-A

52872782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45704778-T-C

52872920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 45704916-T-C

http://identifiers.org/hco/14/GRCh38#52872932-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45704928-C-A

52872942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45704937-T-C

http://identifiers.org/hco/14/GRCh38#52872954-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45704949-C-A

52872967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45704962-C-T

52872976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45704971-C-T

52873037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45705033-G-A

52873037-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45705033-G-T

52873040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45705036-A-G

52873040-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45705036-A-T

http://identifiers.org/hco/14/GRCh38#52873050-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45705046-C-A

52873050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45705046-C-T

52873051-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45705047-T-A

52873051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45705047-T-C

http://identifiers.org/hco/14/GRCh38#52873057-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45705053-A-C

52873057-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45705053-A-T

52873058-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45705054-G-T

52873073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45705069-G-A

52873073-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45705069-G-C

52873073-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45705069-G-T

52873095-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45705083-G-C

52873108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45705096-A-G

52873121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45705109-G-A

52873332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45705245-T-C

http://identifiers.org/hco/14/GRCh38#52873348-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45705256-C-A

52873521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45705379-G-T

52873596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45705438-G-A

http://identifiers.org/hco/14/GRCh38#52873611-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45705447-C-A

52873634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45705471-T-C

52873697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45705523-G-A

52873697-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45705523-G-T

http://identifiers.org/hco/14/GRCh38#52873724-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45705548-C-A

52873840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45705665-G-A

http://identifiers.org/hco/14/GRCh38#52873848-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45705671-C-A

http://identifiers.org/hco/14/GRCh38#52874092-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45705862-A-C

52874092-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45705862-A-G

52874104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45705882-A-G

52874146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45705927-A-G

52874146-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45705927-A-T

52874162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45705943-C-T

52874265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45706042-T-C

http://identifiers.org/hco/14/GRCh38#52874292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45706067-C-A

52874292-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45706067-C-G

52874348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45706114-A-G

52874653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45706385-C-T

52874826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45706526-C-T

http://identifiers.org/hco/14/GRCh38#52875403-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45706878-A-C

52875415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45706890-A-G

52875475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45707165-T-C

52875507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45707204-T-C

52875730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45707400-T-C

52875801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45707502-G-A

52875864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45707540-G-A

52876982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45708600-A-G

52877262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45708769-A-G

52877263-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45708770-T-G

52877319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45708821-T-C

52877357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45708849-G-A

52877357-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45708849-G-T

52877476-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45708959-G-C

52877840-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45709208-C-G

52877840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45709208-C-T

52877920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45709274-C-T

http://identifiers.org/hco/14/GRCh38#52878265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45709565-C-A

52878549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45710198-G-A

52878549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45710198-G-T

http://identifiers.org/hco/14/GRCh38#52878558-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45710205-C-A

52878558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45710205-C-T

52878572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45710219-T-C

http://identifiers.org/hco/14/GRCh38#52878624-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45710271-A-C

52878624-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 45710271-A-T

52878627-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 45710274-C-G

http://identifiers.org/hco/14/GRCh38#52878725-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45710372-A-C

52879693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45712048-A-G

52879851-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45712184-T-G

http://identifiers.org/hco/14/GRCh38#52879965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45712280-C-A

52880320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45712537-G-A

52880358-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45712572-T-A

52880911-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45712943-A-T

52880926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45712958-T-C

52880944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45712968-T-C

http://identifiers.org/hco/14/GRCh38#52881028-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45713022-C-A

52881028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 45713022-C-T

52881215-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45713316-T-A

52881215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45713316-T-C

52881396-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 45713497-G-C

52881417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 45713518-A-G

52881503-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45713600-T-G

52881760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45713840-C-T

52881877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45713956-A-G

http://identifiers.org/hco/14/GRCh38#52881926-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45713997-C-A

52882018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45714066-C-T

52882355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

52882423-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-T

http://identifiers.org/hco/14/GRCh38#52882520-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-C

52882603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-C

52882661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-G

52883388-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45714796-C-G

52883519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45714924-G-A

52885377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45715360-A-G

52885417-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45715401-G-C

52886842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45715559-A-G

52886925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45715645-A-G

http://identifiers.org/hco/14/GRCh38#52886955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45715672-C-A

52887019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45715744-A-G

52888068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45716300-A-G

52888073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45716305-T-C

52888222-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45716432-C-G

52888224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45716434-C-T

52888569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45716601-A-G

52888765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45716748-C-T

52888794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45716777-G-A

52889207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45717089-T-C

52889234-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45717120-G-C

52889414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45717702-G-A

52891552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45719016-A-G

52891921-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45719331-T-A

52892101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45719494-T-C

52893201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45719809-G-T

52893261-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45719858-A-T

http://identifiers.org/hco/14/GRCh38#52893262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45719859-C-A

52893262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45719859-C-T

52893286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 45719882-G-A

52893332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 45719928-C-T

http://identifiers.org/hco/14/GRCh38#52893568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45720145-C-A

52893568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45720145-C-T

52893614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45720251-C-T

52898779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45729519-T-C

52898900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45729616-C-T

52898992-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45729704-G-C

52900075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45730658-T-C

52900891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 45731179-G-A

52900891-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 45731179-G-C

52901432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45731586-G-A

52901527-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45731657-G-C

52901718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45731785-C-T

52902021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45732059-G-A

52902021-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45732059-G-C

52918044-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45740723-A-T

52918080-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45740762-G-C

52918353-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45741198-A-T

52918450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45741248-G-A

52918478-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45741277-A-T

52918615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45741379-G-A

52918630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45741394-G-A

52918805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45741542-T-C

52918838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45741565-T-C

http://identifiers.org/hco/14/GRCh38#52919017-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45741861-C-A

52919017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45741861-C-T

52919304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 45742135-A-G

52919331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 45742162-A-G

52919386-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45742221-T-A

52921998-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45744284-C-G

52922175-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45744462-T-A

52922183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45744469-A-G

http://identifiers.org/hco/14/GRCh38#52922264-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45744529-C-A

52922346-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45744596-T-G

52922388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45744638-T-C

52922521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45744758-G-A

52922686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45744918-T-C

52934728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45750736-T-C

52934840-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45750859-T-A

52934840-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45750859-T-G

52934923-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45750973-C-G

52934948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45750993-T-C

52935222-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45751316-T-G

52935233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45751328-A-G

52935386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45751488-C-T

52935437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45751526-T-C

52935468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45751556-A-G

http://identifiers.org/hco/14/GRCh38#52935647-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45751676-A-C

52935682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45751707-T-C

52935985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45752960-T-C

52936299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45753248-A-G

52937238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45753422-G-A

52937242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45753426-T-C

52937242-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45753426-T-G

52937448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45753600-T-C

52937602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45753748-T-C

52938208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45754254-A-G

52938888-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45755304-G-C

52939943-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45756390-T-G

52940145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45756537-G-A

52941822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45759456-G-A

52941822-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45759456-G-T

52941892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45759515-T-C

52941967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45759590-G-A

52942306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45759884-C-T

52942580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45760155-G-A

52942765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45760307-C-T

52942821-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45760363-C-G

52942955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45760415-G-A

http://identifiers.org/hco/14/GRCh38#52943039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45760498-C-A

52943120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45760557-A-G

52943688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45760965-C-T

http://identifiers.org/hco/14/GRCh38#52943862-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45761117-C-A

52943862-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45761117-C-G

52944397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45762309-A-G

52945819-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45763042-G-C

52946224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45763257-G-A

52946230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45763263-T-C

52946450-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45763439-C-G

52946450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45763439-C-T

52946585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45763530-T-C

52946636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45763588-G-T

52946715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45763654-G-A

52946782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45763716-C-T

http://identifiers.org/hco/14/GRCh38#52947127-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45763990-C-A

52947127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45763990-C-T

52947608-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45764145-T-A

52947900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45764404-T-C

52947943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45764443-C-T

52948104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 45764595-C-T

52948107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 45764598-C-T

52948182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45764667-T-C

52948543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45764925-T-C

52948696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45765061-T-C

http://identifiers.org/hco/14/GRCh38#52948761-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45765117-C-A

52948761-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45765117-C-G

52948793-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45765174-C-G

52949159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45765696-C-T

52949260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45765799-G-A

http://identifiers.org/hco/14/GRCh38#52949283-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45765822-C-A

52949351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45765904-G-A

52949351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45765904-G-T

52949358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45765911-T-C

52949457-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45765942-T-A

52949457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45765942-T-C

52950000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45766502-C-T

http://identifiers.org/hco/14/GRCh38#52950654-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#45767125-C-A

52950654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 45767125-C-T

52950725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45767196-G-A

52950725-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45767196-G-T

http://identifiers.org/hco/14/GRCh38#52950746-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#45767217-C-A

52950746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 45767217-C-T

http://identifiers.org/hco/14/GRCh38#52950789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45767266-C-A

52950789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45767266-C-T

52950844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 45767313-A-G

http://identifiers.org/hco/14/GRCh38#52950854-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45767326-C-A

52950947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 45767406-G-A

http://identifiers.org/hco/14/GRCh38#52950956-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#45767415-C-A

52950956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 45767415-C-T

52950964-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 45767423-G-C

52951014-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 45767454-G-C

52951014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 45767454-G-T

http://identifiers.org/hco/14/GRCh38#52951025-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45767464-C-A

52951062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, undefined
orthologous variants: 45767498-G-A

52951062-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, undefined
orthologous variants: 45767498-G-C

52951251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, undefined
orthologous variants: 45767637-G-A

52951257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, undefined
orthologous variants: 45767643-C-T

52951424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, undefined
orthologous variants: 45767803-G-A

52951533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45767845-T-C

52951533-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45767845-T-G

52951825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45768077-C-T

52951856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45768106-G-A

52951949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45768209-C-T

52952130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45768356-C-T

http://identifiers.org/hco/14/GRCh38#52952172-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45768399-C-A

52952172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45768399-C-T

52952174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45768401-T-C

http://identifiers.org/hco/14/GRCh38#52952175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#45768402-C-A

52952175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15767
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45768402-C-T