14179443-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: 118538968-T-A

http://identifiers.org/hco/18/GRCh38#14179476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118538893-C-A

http://identifiers.org/hco/18/GRCh38#14179631-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118538722-C-A

14179635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118538709-A-G

14179674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118538634-G-A

14179674-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118538634-G-C

14179952-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118538384-T-A

14179952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118538384-T-C

14179958-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118538378-T-A

14179976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118538353-T-C

http://identifiers.org/hco/18/GRCh38#14180084-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118538255-C-A

14180084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118538255-C-T

14180186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118538173-G-A

14180186-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118538173-G-T

http://identifiers.org/hco/18/GRCh38#14180212-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118538152-A-C

14180212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118538152-A-G

14180258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118538109-G-A

14180273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118538090-G-A

14180425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118537706-G-A

14183572-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118536420-T-A

14183572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118536420-T-C

14183613-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118536384-T-A

14183613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118536384-T-C

14183676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118536320-C-T

14183788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118536209-T-C

14183794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118536204-G-A

14183794-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118536204-G-C

14183794-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118536204-G-T

14183795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118536203-A-G

14183799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118536199-G-A

14183799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118536199-G-T

14183813-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118536185-T-A

14183813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118536185-T-C

http://identifiers.org/hco/18/GRCh38#14183829-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118536168-A-C

14183829-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118536168-A-T

14183849-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118536148-T-A

14183849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118536148-T-C

http://identifiers.org/hco/18/GRCh38#14183865-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118536133-C-A

14183873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118536125-A-G

14183937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: 118536062-T-C

http://identifiers.org/hco/18/GRCh38#14183991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118536008-C-A

14184006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: 118535993-C-T

14184013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: 118535986-A-G

14184028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: 118535971-G-A

14184028-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: 118535971-G-C

14184120-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118535882-T-G

14187152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118533831-G-A

14187152-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118533831-G-T

14187158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118533825-T-C

14187163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118533820-T-C

14187163-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118533820-T-G

http://identifiers.org/hco/18/GRCh38#14187203-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118533784-A-C

14187334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118533660-G-A

14187334-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118533660-G-T

14187347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118533647-A-G

14187646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118533397-G-A

14187646-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118533397-G-T

14187670-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118533372-T-A

14187670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118533372-T-C

14187703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118533340-C-T

14187963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118533302-A-G

14187965-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118533300-G-T

14188047-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118533219-G-T

http://identifiers.org/hco/18/GRCh38#14188101-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118533165-A-C

14188101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118533165-A-G

14188117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118533149-G-A

14188117-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118533149-G-C

14188117-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118533149-G-T

14188156-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118533119-G-T

14191855-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 118531231-T-A

14191855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 118531231-T-C

http://identifiers.org/hco/18/GRCh38#14191869-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118531221-C-A

14191869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118531221-C-T

14191875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118531214-A-G

14191922-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118531158-G-C

14191922-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118531158-G-T

14191947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118531142-A-G

14191947-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118531142-A-T

14192035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118531062-A-G

14192037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118531060-A-G

14192037-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118531060-A-T

http://identifiers.org/hco/18/GRCh38#14192053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118531044-C-A

14192053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118531044-C-T

14198402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118529797-T-C

14198461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 118529736-G-A

14198461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 118529736-G-T

14198573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118529605-G-A

14198573-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118529605-G-T

14198592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118529593-G-A

14198592-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118529593-G-C

14198592-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118529593-G-T

14200805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118529463-T-C

14201002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118529276-T-C

14201015-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118529263-G-C

14201015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118529263-G-T

14201019-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118529259-T-A

14201028-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118529250-A-T

14201068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118529065-T-C

14201068-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118529065-T-G

14201099-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118529037-T-G

14201141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118528992-T-C

14201143-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118528990-A-T

14201321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118528837-G-T

14201366-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118528791-T-A

14201434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118528732-A-G

14201698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118528482-G-T

14201725-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118528457-G-T

14201738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118528444-T-C

14201744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118528438-T-C

14206842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118517943-G-A

14206843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118517942-G-A

14206949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118517857-C-T

14206953-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118517853-A-T

14207018-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118517793-G-C

14207114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118517703-A-G

14207114-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118517703-A-T

http://identifiers.org/hco/18/GRCh38#14207263-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118517567-A-C

14207263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118517567-A-G

14207533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118517328-G-A

14207627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118517227-C-T

14207629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118517225-G-A

14207722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118517136-G-A

http://identifiers.org/hco/18/GRCh38#14207904-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118516955-A-C

14207904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118516955-A-G

14207959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118516924-A-G

14208066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: 118516818-T-C

14208116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118516773-A-G

14208122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118516767-T-C

14208217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: 118516670-A-G

14208223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: 118516664-T-C

14208257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118516643-C-T

14208280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118516615-A-G

14208282-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118516613-A-T

14208355-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118516541-A-T

14210481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118513800-G-A

14210482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118513796-T-C

14210534-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118513748-T-A

http://identifiers.org/hco/18/GRCh38#14210700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118513597-C-A

14210738-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118513559-A-T

14210817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118513479-G-A

14210903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118513413-C-T

14213042-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118512823-C-G

14213042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118512823-C-T

http://identifiers.org/hco/18/GRCh38#14213092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118512802-C-A

14213243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118512652-C-T

14213947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118512350-G-A

14213949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118512348-G-A

http://identifiers.org/hco/18/GRCh38#14214016-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118512286-A-C

14214040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118512262-A-G

14214067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118512234-A-G

14214078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118512215-A-G

http://identifiers.org/hco/18/GRCh38#14214080-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118512213-C-A

14214109-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118512185-T-A

14214109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118512185-T-C

14214181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118512134-C-T

http://identifiers.org/hco/18/GRCh38#14214196-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118512119-A-C

14214196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118512119-A-G

14214242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: 118512079-G-A

14214261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: 118512060-G-A

14214261-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: 118512060-G-T

http://identifiers.org/hco/18/GRCh38#14214280-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118512041-A-C

14214280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: 118512041-A-G

http://identifiers.org/hco/18/GRCh38#14214293-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118512028-A-C

14214293-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118512028-A-T

14214967-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118511551-C-G

14214992-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118511526-G-C

14215045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118511491-T-C

14215123-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118511417-C-G

14215282-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118511266-A-T

14215387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118511164-G-A

14215397-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118511160-G-T

14215437-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118511115-T-A

14218373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: 118510410-A-G

14218381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: 118510402-A-G

14218400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: 118510383-T-C

14218428-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: 118510355-C-G

14218466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: 118510317-G-A

14218466-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: 118510317-G-T

14218489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: 118510303-T-C

http://identifiers.org/hco/18/GRCh38#14218491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118510301-C-A

14218491-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: 118510301-C-G

14218491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: 118510301-C-T

14218506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: 118510286-A-G

14218510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: 118510282-G-A

14218581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118510193-G-A

14218581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118510193-G-T

14219821-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118502983-G-T

14219898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118502889-G-A

14219898-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118502889-G-T

14219956-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: 118502831-T-A

14219956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: 118502831-T-C

14219971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: 118502816-A-G

14219971-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: 118502816-A-T

14219972-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: 118502815-T-A

14219972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: 118502815-T-C

14219997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: 118502790-A-G

14219997-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: 118502790-A-T

14220021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: 118502766-G-A

14220144-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118502635-G-T

http://identifiers.org/hco/18/GRCh38#14220169-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118502610-A-C

14220169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118502610-A-G

14220169-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118502610-A-T

14220748-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118501313-T-A

http://identifiers.org/hco/18/GRCh38#14221151-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118500955-C-A

14221205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118500906-G-A

14221205-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118500906-G-T

14221295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: 118500823-T-C

14221330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: 118500788-G-A

14221330-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: 118500788-G-T

14221464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: 118500654-G-A

14221464-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: 118500654-G-T

14221516-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: 118500602-G-T

14221537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: 118500581-G-A

14221537-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: 118500581-G-T

http://identifiers.org/hco/18/GRCh38#14221567-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118500551-A-C

14221579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: 118500539-G-A

14221579-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: 118500539-G-C

14221579-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: 118500539-G-T

14221668-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: 118500452-T-G

14221714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: 118500400-A-G

14221714-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: 118500400-A-T

14225667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant, splice_region_variant
orthologous variants: 118500320-G-A

14225667-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant, splice_region_variant
orthologous variants: 118500320-G-C

14225667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant, splice_region_variant
orthologous variants: 118500320-G-T

http://identifiers.org/hco/18/GRCh38#14225679-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118500308-A-C

14225679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: 118500308-A-G

14225682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: 118500305-A-G

14225682-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: 118500305-A-T

14225723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: 118500264-T-C

14225723-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: 118500264-T-G

14225787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: 118500200-G-T

http://identifiers.org/hco/18/GRCh38#14225865-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118500122-C-A

14225865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: 118500122-C-T

14225904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: 118500083-G-A

14225946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: 118500014-A-G

14225946-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: 118500014-A-T

http://identifiers.org/hco/18/GRCh38#14225970-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118499990-A-C

14225970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: 118499990-A-G

14225985-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: 118499975-A-T

http://identifiers.org/hco/18/GRCh38#14226045-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118499915-C-A

14226045-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: 118499915-C-G

14226051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: 118499909-G-A

14226051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: 118499909-G-T

http://identifiers.org/hco/18/GRCh38#14226071-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118499889-C-A

14226071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118499889-C-T

14227641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: 118498922-G-A

14227641-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: 118498922-G-C

14227641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: 118498922-G-T

14227718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: 118498842-G-T

14227858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118498692-A-G

14228032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118498384-T-C

14228034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118498382-C-T

14228155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118498289-G-A

14228171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118498270-T-C

14228309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118497959-A-G

14228421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118497831-A-G

14228442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118497738-T-C

14228502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118497637-G-A

http://identifiers.org/hco/18/GRCh38#14228507-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118497632-C-A

14228507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118497632-C-T

14228895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118497307-T-C

14229403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118496663-T-C

http://identifiers.org/hco/18/GRCh38#14229431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118496631-C-A

http://identifiers.org/hco/18/GRCh38#14229432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118496630-C-A

14232683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118492696-T-C

14232702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118492684-G-A

14234451-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118488993-T-A

14234451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118488993-T-C

14234533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118488913-A-G

14234556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118488880-C-T

14234578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118488802-A-G

14234651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118488685-A-G

14234651-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118488685-A-T

http://identifiers.org/hco/18/GRCh38#14234774-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118488566-C-A

14234774-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: 118488566-C-G

14234774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: 118488566-C-T

14236747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118488050-G-A

14236747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118488050-G-T

14236766-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118488033-T-G

14236775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118488025-A-G

14236900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118487950-T-C

14236949-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118487913-T-A

14236988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118487882-G-A

14237174-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118487725-T-A

14237202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118487693-A-G

http://identifiers.org/hco/18/GRCh38#14237279-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118487614-C-A

14237279-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118487614-C-G

14237438-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118487467-C-G

http://identifiers.org/hco/18/GRCh38#14237549-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118487364-A-C

http://identifiers.org/hco/18/GRCh38#14237726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118487230-C-A

14237911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118487054-G-T

14237940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118487029-T-C

14242107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118485775-T-C

14242227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: 118485652-T-C

14242297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: 118485582-T-C

http://identifiers.org/hco/18/GRCh38#14242324-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118485553-A-C

14242324-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: 118485553-A-T

14242356-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: 118485521-T-A

14242444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118485436-T-C

14242454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118485426-T-C

14242482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118485404-A-G

14242482-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118485404-A-T

14242509-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118485360-T-G

14242518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118485351-T-C

14242534-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118485329-A-T

14242550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118485306-G-A

14242550-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118485306-G-C

14242550-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118485306-G-T

http://identifiers.org/hco/18/GRCh38#14242556-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118485289-A-C

14242583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118485266-T-C

http://identifiers.org/hco/18/GRCh38#14242970-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118484856-A-C

14242992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118484833-A-G

14243004-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 118484821-T-A

14243004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 118484821-T-C

http://identifiers.org/hco/18/GRCh38#14243032-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118484791-A-C

14243032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: 118484791-A-G

http://identifiers.org/hco/18/GRCh38#14243113-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118484707-C-A

14243113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: 118484707-C-T

14243201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: 118484619-T-C

14243224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: 118484596-G-A

14243224-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: 118484596-G-C

14243228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118484592-G-A

14243228-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118484592-G-T

14243284-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118484541-T-A

14243284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118484541-T-C

14243284-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118484541-T-G

14243320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118484518-A-G

14243342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118484498-G-A

14243342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118484498-G-T

14243495-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118484420-T-A

14243495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118484420-T-C

14243603-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118484286-A-T

14243648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118484214-A-G

14243671-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118484191-G-T

14244029-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118484020-G-C

14244029-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118484020-G-T

14244030-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118484019-G-C

14244248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118483863-G-A

14244295-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118483819-T-A

14244349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118483768-A-G

14244413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118483708-A-G

14244413-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118483708-A-T

http://identifiers.org/hco/18/GRCh38#14244434-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118483687-C-A

http://identifiers.org/hco/18/GRCh38#14244497-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118483625-C-A

14244497-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118483625-C-G

14244497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118483625-C-T

14244501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118483621-T-C

http://identifiers.org/hco/18/GRCh38#14244512-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118483613-C-A

14244512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118483613-C-T

14244518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118483608-A-G

14244556-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 118483569-T-A

14244556-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 118483569-T-C

14244581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: 118483544-A-G

14244581-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: 118483544-A-T

http://identifiers.org/hco/18/GRCh38#14244589-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118483536-C-A

14244589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: 118483536-C-T

14244605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: 118483520-G-A

14244605-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: 118483520-G-C

14244605-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: 118483520-G-T

14244678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: 118483447-A-G

http://identifiers.org/hco/18/GRCh38#14244735-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118483387-C-A

14244735-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: 118483387-C-G

14244735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: 118483387-C-T

14244737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33833
most severe consequence: non coding transcript exon variant
orthologous variants: 118483385-A-G