http://identifiers.org/hco/13/GRCh38#21492966-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#58154358-A-C

21492966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 58154358-A-G

21492966-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 58154358-A-T

21493066-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 58154578-T-G

21493075-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 58154587-T-A

21493075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 58154587-T-C

21493076-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 58154588-T-A

21493076-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 58154588-T-G

21493080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 58154592-T-C

21493091-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 58154603-T-A

21493091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 58154603-T-C

21493091-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 58154603-T-G

http://identifiers.org/hco/13/GRCh38#21493201-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#58154692-A-C

21493216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 58154707-A-G

21493388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58154865-T-C

21494185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58154977-A-G

21494186-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58154978-T-G

21494220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58155015-A-G

http://identifiers.org/hco/13/GRCh38#21494288-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#58155078-C-A

21494288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58155078-C-T

21494311-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58155105-C-G

21494448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58155182-T-C

21495224-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 58156343-A-T

21495302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 58156421-A-G

21495406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58156525-G-A

21495406-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58156525-G-C

21495406-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58156525-G-T

21495453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58156533-A-G

http://identifiers.org/hco/13/GRCh38#21495621-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
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#58156611-C-A

21495621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58156611-C-T

http://identifiers.org/hco/13/GRCh38#21495820-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#58156627-C-A

21495820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 58156627-C-T

21495830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58156637-G-A

21495830-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58156637-G-T

21496246-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58156987-T-A

http://identifiers.org/hco/13/GRCh38#21496289-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#58157092-C-A

21496487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58157377-A-G

21496487-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58157377-A-T

21496492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58157404-G-A

21496492-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58157404-G-T

21496523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58157435-A-G

21502841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58161309-T-C

21502915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58161387-G-A

21502998-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 58161469-T-A

21502998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 58161469-T-C

21502998-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 58161469-T-G

21503102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 58161573-A-G

21503171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58161645-A-G

21503192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58161659-T-C

21503192-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58161659-T-G

21503196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58161663-T-C

21503337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58161770-A-G

http://identifiers.org/hco/13/GRCh38#21503701-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#58162125-C-A

21503845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58162264-C-T

21504218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58162627-C-T

21509226-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58163414-C-G

21509261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58163450-A-G

21509294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58163479-T-C

21509295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58163480-G-A

21509650-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58163943-T-A

21509715-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58163978-A-T

21509786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58164050-T-C

21509844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58164102-A-G

http://identifiers.org/hco/13/GRCh38#21509916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#58164360-C-A

21509922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58164366-T-C

21509953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58164395-T-C

21509956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58164398-T-C

21514437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58169779-T-C

http://identifiers.org/hco/13/GRCh38#21515424-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#58170062-C-A

21515424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58170062-C-T

21515433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58170071-T-C

http://identifiers.org/hco/13/GRCh38#21515480-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#58170108-C-A

21515480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58170108-C-T

21516170-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58170753-T-A

21516471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58171005-T-C

21516531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58171058-T-C

21516579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58171108-C-T

21516585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58171114-A-G

21516750-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58175773-T-A

21516756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58175779-C-T

21516873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58175884-T-C

21516930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58175941-A-G

21517048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58176057-C-T

21517952-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-T

21517959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-G

21520791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58180414-C-T

21521104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58180718-A-G

21521181-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58180985-T-G

http://identifiers.org/hco/13/GRCh38#21521194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#58180998-C-A

21521194-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58180998-C-G

21521194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58180998-C-T

http://identifiers.org/hco/13/GRCh38#21521266-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#58181066-A-C

21521266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 58181066-A-G

21521266-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 58181066-A-T

21521335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 58181135-G-A

21521350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58181154-T-C

21521382-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58181186-T-A

21521382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58181186-T-C

21521409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58181213-T-C

21521409-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58181213-T-G

21521453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58181263-A-G

21521585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58181363-T-C

21521784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58181556-T-C

21521785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58181557-T-C

http://identifiers.org/hco/13/GRCh38#21521926-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#58181688-C-A

21521939-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58181701-C-G

21521939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58181701-C-T

21522590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58182824-G-A

21522760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58182996-C-T

21523050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58183251-G-A

21523094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58183289-C-T

21523099-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58183299-T-G

21527297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58185017-C-T

21527519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58185248-A-G

21527598-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58185316-T-G

21528150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58185862-T-C

http://identifiers.org/hco/13/GRCh38#21528169-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#58185875-A-C

21528345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58186003-G-A

21537174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58187056-G-A

21537231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58187114-C-T

21537268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58187149-A-G

21537430-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58187320-T-A

21537430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58187320-T-C

21539011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58191230-C-T

21539184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58191416-T-C

21539217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58191455-G-A

21539217-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58191455-G-T

21539275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58191570-A-G

21539347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 58191638-T-C

http://identifiers.org/hco/13/GRCh38#21539392-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#58191683-A-C

21539392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58191683-A-G

21539392-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58191683-A-T

21539428-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58191727-A-T

21539661-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 58192460-T-A

21539753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58192551-A-G

21539988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58192773-T-C

21540760-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58194712-A-T

http://identifiers.org/hco/13/GRCh38#21540768-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#58194720-A-C

http://identifiers.org/hco/13/GRCh38#21540861-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#58194808-A-C

21541064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58195324-G-A

http://identifiers.org/hco/13/GRCh38#21541358-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#58195543-A-C

21541549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58195736-T-C

21541628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58195816-A-G

21541731-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58195915-T-A

21541744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58195928-C-T

21548027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58197938-T-C

21548129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58198061-A-G

21550601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58199709-G-A

21550606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58199714-T-C

21550615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58199723-G-A

21550615-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58199723-G-C

21550831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58199958-G-A

21550899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58199995-G-A

21551254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58200296-A-G

http://identifiers.org/hco/13/GRCh38#21551261-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#58200303-C-A

21551261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58200303-C-T

21556015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58200963-A-G

http://identifiers.org/hco/13/GRCh38#21556138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#58201082-C-A

21556138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58201082-C-T

http://identifiers.org/hco/13/GRCh38#21556220-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#58201137-A-C

21556220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58201137-A-G

21556302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58201215-T-C

21556386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58201289-C-T

21556583-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58201456-G-C

21556652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58201517-G-A

21556665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58201530-T-C

21556665-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58201530-T-G

21556730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58201594-T-C

21557054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58201889-G-A

21557262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58202074-A-G

21557325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58202111-A-G

21557369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58202136-G-A

21557369-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58202136-G-C

21557459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58202177-G-A

http://identifiers.org/hco/13/GRCh38#21558112-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#58202806-C-A

21558112-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58202806-C-G

21558397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58203158-T-C

21558486-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58203245-C-G

21564965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-C

21564965-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-G

21564970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-C

21565018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

http://identifiers.org/hco/13/GRCh38#21566055-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#58207844-A-C

21566373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58208092-C-T

21566495-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58208221-G-C

21566495-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58208221-G-T

21566505-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58208230-T-A

21566505-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58208230-T-G

21566837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 58209148-T-C

21566859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 58209170-T-C

21568955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58209979-A-G

21569342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58210348-C-T

21569358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58210364-A-G

21570008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58210873-A-G

21570018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58210882-T-C

21570047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58210910-A-G

21570106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58210969-C-T

http://identifiers.org/hco/13/GRCh38#21570183-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#58211041-A-C

21570394-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58211213-A-T

21570411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58211233-T-C

21570483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58211309-G-A

21570483-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58211309-G-C

21570617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58211430-C-T

21572811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58213037-T-C

21574223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58215903-A-G

21574380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58216069-T-C

21574679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58216385-T-C

21574767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58216475-T-C

21575054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58216749-T-C

21575354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58217013-T-C

http://identifiers.org/hco/13/GRCh38#21575355-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#58217014-A-C

http://identifiers.org/hco/13/GRCh38#21575759-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#58217046-C-A

21575759-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58217046-C-G

21575762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58217049-G-A

21575762-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58217049-G-T

21575906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58217190-G-A

21576408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58217685-T-C

21576763-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58218044-A-T

http://identifiers.org/hco/13/GRCh38#21578287-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#58218860-C-A

21578786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58219267-C-T

21580077-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58220057-T-G

21580147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58220141-A-G

http://identifiers.org/hco/13/GRCh38#21580393-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#58220996-A-C

21580426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58221202-T-C

21580508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58221281-A-G

21580638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58221407-G-A

21580638-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58221407-G-C

21580638-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58221407-G-T

21582402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58222699-A-G

21582431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58222724-T-C

21583681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58223451-A-G

21583765-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58223532-G-T

21583835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58223609-G-A

21583835-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58223609-G-C

21583864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58223640-A-G

21584713-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58224108-T-A

21584869-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58224174-T-A

21585016-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58224293-G-C

http://identifiers.org/hco/13/GRCh38#21585054-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#58224341-C-A

21585469-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58224731-A-T

21585554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58224810-T-C

21587322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58225435-A-G

21587371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58225484-T-C

21587384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58225495-T-C

21587458-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58225553-C-G

21587564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58225633-T-C

21595131-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58229252-G-C

21595535-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58229654-G-C

21595804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58229824-G-A

21595865-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58229868-T-A

21597322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58231183-C-T

21597344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58231205-T-C

21597489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58231320-A-G

21599546-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58231774-T-A

21599546-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58231774-T-G

21599905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58232089-G-A

21600395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58234246-G-A

21600433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58234284-T-C

21600549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58234372-T-C

21600696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58234479-T-C

21600745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58234529-T-C

21601399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58234793-G-A

21601399-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58234793-G-C

http://identifiers.org/hco/13/GRCh38#21603433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#58236193-C-A

21603433-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58236193-C-G

21603500-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58236255-A-T

http://identifiers.org/hco/13/GRCh38#21603543-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#58236280-C-A

http://identifiers.org/hco/13/GRCh38#21603545-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#58236282-C-A

21603545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58236282-C-T

21603551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58236288-G-A

21603551-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58236288-G-T

21603553-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58236290-T-A

21603553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58236290-T-C

21603553-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58236290-T-G

21603565-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58236302-T-A

http://identifiers.org/hco/13/GRCh38#21603592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#58236328-C-A

21603592-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58236328-C-G

21603592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58236328-C-T

21603683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58236361-G-A

21603683-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58236361-G-C

21603683-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58236361-G-T

21603684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58236362-T-C

21603762-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58236410-G-T

http://identifiers.org/hco/13/GRCh38#21603787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#58236422-C-A

21603787-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58236422-C-G

21603787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58236422-C-T

21603822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58236429-G-A

21603934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58236482-T-C

21603934-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58236482-T-G

21604075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 58236623-C-T

http://identifiers.org/hco/13/GRCh38#21604113-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#58236661-C-A

21604113-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 58236661-C-G

21604113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 58236661-C-T

21604121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 58236669-G-A

21604121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31830
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 58236669-G-T