53267510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: 3 prime UTR variant
orthologous variants: 77891685-G-A

http://identifiers.org/hco/6/GRCh38#53267883-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77891319-C-A

53267898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: 3 prime UTR variant
orthologous variants: 77891304-T-C

53267963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: 3 prime UTR variant
orthologous variants: 77891253-A-G

53268199-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: 3 prime UTR variant
orthologous variants: 77891028-T-G

53268220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: 3 prime UTR variant
orthologous variants: 77891000-C-T

53268635-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: 3 prime UTR variant
orthologous variants: 77890584-T-G

53269196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: missense_variant, synonymous_variant
orthologous variants: 77890019-C-T

53269233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: missense_variant, synonymous_variant
orthologous variants: 77889982-T-C

53269302-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron variant
orthologous variants: 77889914-T-A

53269302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron variant
orthologous variants: 77889914-T-C

http://identifiers.org/hco/6/GRCh38#53269332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77889897-C-A

53269332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron variant
orthologous variants: 77889897-C-T

http://identifiers.org/hco/6/GRCh38#53269358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77889877-C-A

53269358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron variant
orthologous variants: 77889877-C-T

53269385-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron variant
orthologous variants: 77889849-G-T

http://identifiers.org/hco/6/GRCh38#53269389-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77889845-A-C

53269389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron variant
orthologous variants: 77889845-A-G

53269389-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron variant
orthologous variants: 77889845-A-T

53269932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron variant
orthologous variants: 77889398-T-C

53270512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron variant
orthologous variants: 77888946-A-G

53270512-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron variant
orthologous variants: 77888946-A-T

53270575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron variant
orthologous variants: 77888906-G-A

http://identifiers.org/hco/6/GRCh38#53270882-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77888645-C-A

53270882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron variant
orthologous variants: 77888645-C-T

53270893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron variant
orthologous variants: 77888633-T-C

http://identifiers.org/hco/6/GRCh38#53270894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77888632-C-A

53270920-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron variant
orthologous variants: 77888606-T-A

53270920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron variant
orthologous variants: 77888606-T-C

53270920-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron variant
orthologous variants: 77888606-T-G

53272223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron variant
orthologous variants: 77887950-G-A

53272615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron variant
orthologous variants: 77887763-T-C

53272703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron variant
orthologous variants: 77887706-G-A

53272883-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron variant
orthologous variants: 77887517-T-G

53272941-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron variant
orthologous variants: 77887467-T-G

53273185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron variant
orthologous variants: 77887263-A-G

http://identifiers.org/hco/6/GRCh38#53273396-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77887057-A-C

53273396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron variant
orthologous variants: 77887057-A-G

53273397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron variant
orthologous variants: 77887056-A-G

53273397-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron variant
orthologous variants: 77887056-A-T

53273400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron variant
orthologous variants: 77887053-G-A

53273400-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron variant
orthologous variants: 77887053-G-C

53273400-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron variant
orthologous variants: 77887053-G-T

53273424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron variant
orthologous variants: 77887037-A-G

http://identifiers.org/hco/6/GRCh38#53273429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77887032-C-A

53273429-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron variant
orthologous variants: 77887032-C-G

53273449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron variant
orthologous variants: 77887019-G-A

53273449-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron variant
orthologous variants: 77887019-G-T

53273455-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron variant
orthologous variants: 77887013-T-A

53273455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron variant
orthologous variants: 77887013-T-C

53273455-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron variant
orthologous variants: 77887013-T-G

53273480-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron variant
orthologous variants: 77886982-A-T

53273873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron variant
orthologous variants: 77886764-G-T

53274102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron variant
orthologous variants: 77886570-T-C

http://identifiers.org/hco/6/GRCh38#53274103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77886569-C-A

http://identifiers.org/hco/6/GRCh38#53274213-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77886464-A-C

53274338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron variant
orthologous variants: 77886376-C-T

53274466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron variant
orthologous variants: 77886272-T-C

53274489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron variant
orthologous variants: 77886245-T-C

53274506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron variant
orthologous variants: 77886230-G-A

53274703-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron variant
orthologous variants: 77886106-G-C

53274722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron variant
orthologous variants: 77886085-G-A

53274941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron variant
orthologous variants: 77885881-G-A

53274941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron variant
orthologous variants: 77885881-G-T

53275011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron variant
orthologous variants: 77884268-G-A

53275011-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron variant
orthologous variants: 77884268-G-T

http://identifiers.org/hco/6/GRCh38#53275012-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77884267-C-A

http://identifiers.org/hco/6/GRCh38#53275251-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#77884038-A-C

53275251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 77884038-A-G

53275776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77883526-G-A

53275827-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77883467-T-A

53275842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77883452-C-T

53275985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77883351-T-C

53276008-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77883324-T-G

53276074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77883261-G-T

53276092-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77883243-A-G

53276095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77883240-T-C

53276095-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77883240-T-G

53276106-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77883229-T-A

53276119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77883216-C-T

53276142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77883192-A-G

53276153-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77883181-T-C

53276159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77883166-T-C

53276213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77883108-T-C

53276268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77883053-G-A

53276268-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77883053-G-C

53276298-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77883024-C-G

53276341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77882988-A-G

53276374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77882955-G-T

http://identifiers.org/hco/6/GRCh38#53276388-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77882941-C-A

53276388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77882941-C-T

53276487-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77882843-G-C

53276501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77882832-C-T

53276722-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77882686-T-G

53276754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77882652-C-T

53276818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77882603-G-A

53277176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77878436-A-G

http://identifiers.org/hco/6/GRCh38#53277182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77878430-C-A

53277183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77878429-C-T

53277207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77878405-A-G

53277312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77878296-C-T

53277523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77878132-G-A

53277596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77878072-A-G

53277734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77877951-A-G

http://identifiers.org/hco/6/GRCh38#53277736-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77877949-C-A

53277736-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77877949-C-G

53277736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77877949-C-T

53277786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77877904-G-A

53277786-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77877904-G-T

53277819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77877871-A-G

http://identifiers.org/hco/6/GRCh38#53278432-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77877325-A-C

53278482-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77877286-T-A

53278482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77877286-T-C

53278483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77877285-T-C

53278540-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77877230-A-T

53278582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77877193-T-C

http://identifiers.org/hco/6/GRCh38#53278720-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77877073-A-C

53279022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77876809-G-A

53279115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77876747-G-A

53279190-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77876646-T-A

53279204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77876632-C-T

53279288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77876554-T-C

53279403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77876432-T-C

53279403-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77876432-T-G

53279404-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77876431-C-G

53279550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77876248-G-A

53279666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77875906-T-C

53280058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77875522-G-A

53280103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77875476-A-G

53280159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77875442-G-A

53280159-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77875442-G-C

53280167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77875434-G-A

53281084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77874875-C-T

53281187-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77874794-G-T

53281191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77874790-G-A

53281278-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77874704-G-C

http://identifiers.org/hco/6/GRCh38#53281605-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77874478-A-C

53281605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77874478-A-G

53281627-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77874463-A-T

http://identifiers.org/hco/6/GRCh38#53282137-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77874135-C-A

53282137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77874135-C-T

53282155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77874117-T-C

53282192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77874072-T-C

53282667-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77873232-T-A

53282735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77873164-T-C

53282735-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77873164-T-G

53283201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77872771-C-T

53283311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77872658-C-T

53287420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77871919-A-G

53287486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77871849-A-G

53287523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77871831-G-A

53287542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77871814-C-T

53287718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77871766-G-T

53287719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77871765-T-C

53287745-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77871740-G-T

53287774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77871715-G-A

53287794-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77871699-G-C

http://identifiers.org/hco/6/GRCh38#53287856-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#77871659-A-C

http://identifiers.org/hco/6/GRCh38#53287880-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77871636-C-A

53287880-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 77871636-C-G

53287903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained, undefined
orthologous variants: 77871614-G-A

53287903-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 77871614-G-C

53287943-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 77871575-C-G

53287970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77871545-T-C

53288047-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77871467-T-A

53288047-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77871467-T-G

53288058-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77871456-G-T

http://identifiers.org/hco/6/GRCh38#53288075-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77871439-A-C

53288075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77871439-A-G

53288075-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77871439-A-T

53288081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77871433-A-G

http://identifiers.org/hco/6/GRCh38#53288084-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77871430-A-C

53288595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77870734-C-T

http://identifiers.org/hco/6/GRCh38#53289137-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77870521-C-A

53289202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77870461-T-C

53290220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77869923-T-C

53290427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77869702-T-C

53290472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77869657-G-A

53290474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77869655-G-T

http://identifiers.org/hco/6/GRCh38#53290547-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77869586-C-A

http://identifiers.org/hco/6/GRCh38#53290659-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77869395-A-C

53290669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77869390-G-T

53290868-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77869260-C-G

53291622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77868482-G-A

53291676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77868435-A-G

53291692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77868414-C-T

http://identifiers.org/hco/6/GRCh38#53291936-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77868173-A-C

53292117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77868023-T-C

53292119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77868021-C-T

53292283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77867877-T-C

53292328-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77867835-T-C

53292373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77867807-T-C

53292402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77867778-G-A

53292412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77867768-G-A

53293679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77867275-C-T

53293725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77867242-C-T

53293753-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77867214-T-G

53293794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77867177-T-C

53293836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77867133-C-T

53293864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77867104-G-A

53293864-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77867104-G-C

53293941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77867054-A-G

53293941-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77867054-A-T

53294034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77866965-T-C

53294214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77866850-C-T

53294254-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77866809-G-T

http://identifiers.org/hco/6/GRCh38#53294376-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77866726-A-C

53294376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 77866726-A-G

http://identifiers.org/hco/6/GRCh38#53294523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77866609-C-A

53294523-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77866609-C-G

53294569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77866569-T-C

http://identifiers.org/hco/6/GRCh38#53294798-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77866206-A-C

http://identifiers.org/hco/6/GRCh38#53294832-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77866174-A-C

53294884-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77866131-T-G

53295036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77865984-C-T

53295057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77865964-G-A

53295400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77864732-A-G

http://identifiers.org/hco/6/GRCh38#53295441-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77864670-C-A

53295508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77864613-T-C

53295534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77864587-T-C

53295809-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77864320-G-T

53295812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77864317-A-G

53295825-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77864308-G-C

53295825-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77864308-G-T

53295834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77864299-G-A

53295834-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77864299-G-T

53295986-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77864109-C-G

53298811-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77863059-T-A

53298906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77862980-G-A

53298906-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77862980-G-C

53298906-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77862980-G-T

53298920-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77862970-T-A

53298920-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77862970-T-G

53299103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77862809-T-C

53299123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77862789-A-G

53299182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77862756-T-C

53299182-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77862756-T-G

53299237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77862699-G-A

53299264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77862672-T-C

53299266-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77862670-T-G

53299287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77862643-A-G

53299497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77862445-G-A

53300027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77862029-G-A

http://identifiers.org/hco/6/GRCh38#53300046-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77862014-C-A

http://identifiers.org/hco/6/GRCh38#53300118-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77861958-A-C

53300119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77861957-T-C

53300124-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77861952-A-T

53300336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77861757-C-T

53300358-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77861733-C-G

53300809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77860890-G-A

53300818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77860881-G-A

53300823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77860876-C-T

53301000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77860718-A-G

53301217-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77860520-G-C

53301217-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77860520-G-T

53301487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77860295-C-T

53301604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77860185-G-A

53301840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77859838-T-C

53302111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77859461-G-A

53302651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77858585-G-A

53302834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77858439-T-C

53302836-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77858437-C-G

53302842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77858431-G-A

53302885-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77858388-T-A

53302885-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77858388-T-G

53303186-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77858102-C-G

53303186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77858102-C-T

53303298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77857905-T-C

53303577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77857697-A-G

53303809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77857458-G-A

53303809-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77857458-G-T

53303856-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77857418-G-C

http://identifiers.org/hco/6/GRCh38#53306751-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77856280-A-C

53306751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77856280-A-G

53306809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77856226-T-C

53306998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77856053-G-A

53307128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77855942-T-C

53307131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77855939-C-T

http://identifiers.org/hco/6/GRCh38#53307420-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77855672-A-C

53307569-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77855576-C-G

53307800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77855356-A-G

53307830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77855330-C-T

53307833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77855327-C-T

53314245-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77849183-T-G

53314839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77848700-T-C

53314839-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77848700-T-G

53315055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77848497-T-C

53315071-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77848481-T-A

53315071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77848481-T-C

53322372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77847751-A-G

53322626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77847530-T-C

53322889-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77847289-T-G

53323015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77847194-A-G

53331713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77841657-T-C

http://identifiers.org/hco/6/GRCh38#53331746-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77841623-A-C

53332984-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77840852-G-C

53333292-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77840287-G-C

53333319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77840259-T-C

53333341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77840237-A-G

http://identifiers.org/hco/6/GRCh38#53333653-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77839920-A-C

53333672-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77839901-A-T

53333720-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77839853-T-A

53333783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77839795-A-G

53334044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77839679-T-C

53334214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77839573-A-G

53334327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77839456-C-T

53334402-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77839383-T-A

53335077-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77835123-C-G

53335105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77835091-A-G

53335280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77834963-G-A

53335320-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77834925-T-A

53335320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77834925-T-C

53335335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77834910-G-A

53335335-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77834910-G-C

53335359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77834893-A-G

53335376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77834877-T-C

53335390-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77834864-C-G

53336723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77834382-G-A

http://identifiers.org/hco/6/GRCh38#53336804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77834301-C-A

53336804-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77834301-C-G

53338031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77833329-G-A

53338031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77833329-G-T

53338099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77833269-G-A

53338262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77833132-G-A

53338262-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77833132-G-C

53338275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77833120-A-G

http://identifiers.org/hco/6/GRCh38#53338476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77832653-C-A

53338476-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77832653-C-G

53338477-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77832652-T-G

53338511-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77832620-C-G

53338612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77832530-A-G

53338628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77832514-C-T

53339235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77831939-T-C

53339423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77831756-T-C

53340935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77831600-C-T

53340977-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77831560-A-T

53341035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77831495-T-C

53341108-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77831413-G-C

53341196-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77831329-G-C

53341287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77831239-T-C

53341306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77831226-C-T

53341542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77831032-G-A

53341786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77830805-C-T

53341867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77830732-T-C

53341920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77830684-G-A

53341998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77830614-G-A

53342118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77830469-C-T

53342511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77830099-T-C

53342770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77829866-A-G

53342775-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77829861-C-G

53344395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77828799-T-C

53344441-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77828752-T-C

53344785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77828406-T-C

53344810-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77828384-A-T

53344875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77828347-A-G

53345355-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77828017-C-G

http://identifiers.org/hco/6/GRCh38#53345526-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77827867-C-A

53346780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77826456-T-C

53347174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77826103-T-C

53347174-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77826103-T-G

53347208-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77826078-A-T

53347341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77825938-C-T

53347350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77825930-T-C

53347350-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77825930-T-G

http://identifiers.org/hco/6/GRCh38#53347415-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77825865-C-A

53347752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77825521-T-C

53347807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77825461-A-G

53347894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77825386-G-A

53348255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77825172-G-A

53348522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77824989-G-T

53348840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 77824782-A-G

http://identifiers.org/hco/6/GRCh38#53348887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77824740-C-A

53348887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 77824740-C-T

53349128-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: 5 prime UTR variant
orthologous variants: 77824518-G-C

53349128-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: 5 prime UTR variant
orthologous variants: 77824518-G-T

http://identifiers.org/hco/6/GRCh38#53349145-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77824501-C-A

53349145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21308
most severe consequence: 5 prime UTR variant
orthologous variants: 77824501-C-T