http://identifiers.org/hco/12/GRCh38#14365753-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#136495887-C-A

14365753-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 136495887-C-G

14365753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 136495887-C-T

14365773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 136495907-G-A

14365773-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 136495907-G-T

14365795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 136495929-T-C

14365927-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 136496061-G-T

14366184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136496317-C-T

14366475-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136496600-G-C

14366547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136496676-T-C

14366791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 136496874-A-G

14366800-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 136496883-C-G

14366806-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136496890-G-T

14367019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 136497076-A-G

14367141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 136497209-C-T

14367364-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 136497451-T-A

14367364-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 136497451-T-G

14367394-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 136497484-C-G

14367399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 136497489-G-A

http://identifiers.org/hco/12/GRCh38#14367429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#136497518-C-A

14367446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 136497528-A-G

14367683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136497660-G-A

14367695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136497672-A-G

14367957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136497936-G-A

14367957-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136497936-G-T

14368170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136498090-A-G

14368198-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136498106-T-A

14368198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136498106-T-C

14369187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 136499480-A-G

14369343-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136499621-T-G

14370514-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136500465-G-T

http://identifiers.org/hco/12/GRCh38#14370610-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#136500542-C-A

14370614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136500554-G-A

14370676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136500624-T-C

14370798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136500739-A-G

14370918-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136500993-A-T

14371209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136501315-C-T

14371368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136501499-A-G

14378701-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136503996-G-C

14383976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136508733-C-T

14384129-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136508864-C-G

14384129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136508864-C-T

14384212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136508933-A-G

14384377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136509070-G-A

14384863-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 136509507-T-A

14385008-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 136509663-G-T

14385033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 136509688-G-A

14385033-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 136509688-G-C

14385366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 136510017-A-G

14385969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136510577-C-T

14385996-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136510641-T-A

http://identifiers.org/hco/12/GRCh38#14386074-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#136510719-A-C

14386994-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136512010-G-T

14387469-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136512508-A-T

14387775-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136512760-G-C

14387780-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136512765-A-T

14387887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136512871-C-T

14389403-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136513180-G-C

14389407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136513184-A-G

14390430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136513926-C-T

14390876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136514470-C-T

14390926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 136514596-A-G

14391100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 136514739-G-A

14391100-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 136514739-G-C

14391478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136515067-T-C

14391516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136515091-A-G

14392927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136515800-T-C

14392931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136515804-A-G

14393129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136515991-A-G

14394064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136519799-G-A

14394101-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136519836-G-C

14394295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136520016-C-T

14394976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 136520633-A-G

14395042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 136520710-G-A

14395515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136521138-C-T

14395570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 136521166-A-G

14395769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136521356-G-T

14395933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 136521493-T-C

http://identifiers.org/hco/12/GRCh38#14396208-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#136521747-C-A

14396649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 136522158-A-G

14396822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136522324-A-G

14396898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136522405-C-T

14398254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136523553-T-C

14398294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136523585-T-C

14398474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136523746-G-A

14398474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136523746-G-T

14398660-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136523915-T-A

14402576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136524762-G-A

14402576-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136524762-G-T

14403379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136525149-G-A

14406589-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136526576-A-T

14407682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136527391-C-T

14408049-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136527707-C-G

14408078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136527736-G-A

14408113-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136527789-T-G

14408115-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136527791-T-G

14408282-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136527952-C-G

14408282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136527952-C-T

14408615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136528286-G-A

14408908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136528559-C-T

14408943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136528593-G-A

14409328-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136528921-T-A

14409536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136529074-T-C

14409583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136529103-G-A

14409684-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136529197-G-T

14409720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136529233-A-G

14416291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136530410-C-T

14416385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136530503-A-G

14416618-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136530713-G-C

http://identifiers.org/hco/12/GRCh38#14416855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#136530985-C-A

http://identifiers.org/hco/12/GRCh38#14417788-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#136531861-C-A

14417789-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136531862-A-T

http://identifiers.org/hco/12/GRCh38#14417799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#136531872-C-A

14418048-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 136532127-A-T

14418202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 136532256-A-G

http://identifiers.org/hco/12/GRCh38#14418326-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#136532383-A-C

14418511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 136532574-A-G

14418774-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136532833-T-G

14419168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 136533351-G-A

14419215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 136533423-T-C

14419448-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136533732-G-T

14419543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136533818-A-G

14419576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136533847-T-C

14419970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136534185-T-C

14420015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 136534231-T-C

http://identifiers.org/hco/12/GRCh38#14420050-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#136534243-C-A

http://identifiers.org/hco/12/GRCh38#14423768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#136536630-C-A

14423768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 136536630-C-T

14423781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 136536643-G-A

14423781-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 136536643-G-T

14424454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136537331-C-T

14424485-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 136537362-C-G

14424487-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136537364-C-G

14424487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136537364-C-T

14424488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 136537365-T-C

14424500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 136537377-T-C

14424500-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 136537377-T-G

14424502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136537379-C-T

14424513-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136537390-T-A

14424689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 136537629-T-C

14424838-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136537805-C-G

14424868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136537835-A-G

14424952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136537919-A-G

14424953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 136537920-T-C

14425420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136538384-C-T

14425451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 136538415-G-A

14425451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 136538415-G-T

14425496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136538448-A-G

14425499-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136538451-G-T

14425529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136538481-A-G

http://identifiers.org/hco/12/GRCh38#14425544-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#136538497-A-C

14425544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136538497-A-G

14429003-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136538811-A-T

14429015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136538827-G-A

14429015-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136538827-G-C

14429015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136538827-G-T

14429052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136538875-A-G

14434053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136540501-T-C

14434110-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136540554-T-G

14434179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136540598-G-A

14434179-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136540598-G-C

14434180-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136540599-T-G

14434208-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136540626-T-A

14434208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136540626-T-C

http://identifiers.org/hco/12/GRCh38#14434285-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#136540704-C-A

14434292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136540711-G-A

14434361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136540779-A-G

14435470-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136541389-C-G

14435847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136541761-A-G

14436000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136541906-G-A

http://identifiers.org/hco/12/GRCh38#14436007-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#136541914-C-A

14436007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136541914-C-T

14436017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136541924-A-G

14436021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136541928-A-G

14436086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136541993-A-G

http://identifiers.org/hco/12/GRCh38#14436221-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#136542130-C-A

14436221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 136542130-C-T

14436255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136542173-T-C

14436263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136542181-A-G

14436281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136542208-T-C

14437628-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136543462-G-C

14437727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136543555-G-A

14438400-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136543929-G-T

14438494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136544028-G-T

14438556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136544091-A-G

14438556-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136544091-A-T

14438717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136544248-T-C

14446586-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136548104-T-G

14446609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136548127-A-G

14446610-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136548128-C-G

14446820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136548337-A-G

http://identifiers.org/hco/12/GRCh38#14446848-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#136548360-C-A

14446889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136548392-G-A

14446889-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136548392-G-T

14446910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136548414-A-G

14446910-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136548414-A-T

14446927-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136548423-T-A

14446927-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136548423-T-G

14446936-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136548432-G-C

14446936-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136548432-G-T

14447063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136548545-T-C

http://identifiers.org/hco/12/GRCh38#14456424-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#136552097-C-A

http://identifiers.org/hco/12/GRCh38#14456429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#136552102-C-A

http://identifiers.org/hco/12/GRCh38#14456482-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#136552162-A-C

14456491-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136552171-T-A

14457413-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136559592-T-A

14457497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136559666-G-A

http://identifiers.org/hco/12/GRCh38#14457638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#136559779-C-A

14457723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136559887-A-G

14457744-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136559902-A-T

14457864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136560046-G-A

14457945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136560151-T-C

14459648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136563252-G-A

14460412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136563951-T-C

14460441-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136563992-A-T

14460456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136564007-A-G

14460456-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136564007-A-T

14460484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136564033-T-C

14460513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 136564061-T-C

14460513-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136564061-T-G

14460568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 136564116-G-A

http://identifiers.org/hco/12/GRCh38#14460646-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#136564194-A-C

14460774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136564322-A-G

14460859-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 136564407-C-G

14460943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 136564491-A-G

14460952-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 136564500-G-T

14461044-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136564592-A-T

14461091-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136564639-T-A

14461215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136564741-G-A

14461215-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136564741-G-T

14461268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136564792-A-G

14461275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136564799-T-C

http://identifiers.org/hco/12/GRCh38#14461276-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#136564800-A-C

14461276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136564800-A-G

14461708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136565622-G-A

http://identifiers.org/hco/12/GRCh38#14462371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#136566135-C-A

14462969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136566709-T-C

14463532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136567249-G-A

14463617-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136567333-G-C

14463812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136567527-G-A

14464340-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136568253-C-G

14464466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136568381-G-A

14466119-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136569504-T-A

14466119-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136569504-T-G

http://identifiers.org/hco/12/GRCh38#14466166-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#136569548-A-C

14466522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 136570076-T-C

14475075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136572532-A-G

http://identifiers.org/hco/12/GRCh38#14475177-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#136572633-A-C

14475588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136572941-T-C

14475979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136573522-A-G

14475979-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136573522-A-T

14476451-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136574562-T-A

14476459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136574570-G-A

14476459-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136574570-G-T

14476538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136574617-T-C

14476543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136574622-C-T

http://identifiers.org/hco/12/GRCh38#14476554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#136574640-C-A

14476554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136574640-C-T

14476586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136574670-G-A

14476660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136574759-T-C

14476740-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136574833-G-T

14476840-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136574916-A-T

14476896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136574966-C-T

14477305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136575333-T-C

14477331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136575359-G-A

14477356-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136575384-A-T

14477636-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136575643-C-G

14477783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136575772-T-C

14477784-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136575773-T-G

14478189-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136576521-A-T

http://identifiers.org/hco/12/GRCh38#14478302-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#136576633-A-C

14478302-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136576633-A-T

14478343-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136576674-G-C

14478343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136576674-G-T

14478345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 136576676-A-G

14478381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 136576712-A-G

14478381-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 136576712-A-T

14478479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 136576810-T-C

14479410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136577568-C-T

14480911-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136580192-T-G

14480927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136580208-G-A

14480927-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136580208-G-C

14480927-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136580208-G-T

http://identifiers.org/hco/12/GRCh38#14480945-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#136580226-C-A

14480945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136580226-C-T

14480947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136580228-G-T

14480949-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136580230-T-A

14481025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 136580305-A-G

14481166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 136580446-G-A

14481226-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 136580508-G-T

14481624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 136580721-A-G

14481635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 136580735-G-A

14481655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 136580755-T-C

http://identifiers.org/hco/12/GRCh38#14481813-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#136581008-A-C

14481921-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 136581081-T-A

14481950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 136581104-A-G

14482027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 136581146-A-G

14495654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136581672-A-G

14495890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136582120-C-T

14495975-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136582194-A-G

http://identifiers.org/hco/12/GRCh38#14496084-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#136582251-A-C

http://identifiers.org/hco/12/GRCh38#14496137-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#136582303-C-A

14496137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136582303-C-T

14496138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136582304-A-G

14496152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136582318-T-C

14496152-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136582318-T-G

14496200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136582356-T-C

14496228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 136582377-T-C

14496262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 136582411-A-G

14496262-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 136582411-A-T

14497568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136583400-G-A

14497568-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136583400-G-C

14497568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136583400-G-T

14497648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 136583466-C-T

http://identifiers.org/hco/12/GRCh38#14498151-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#136583968-A-C

14498186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136584004-G-A

14498186-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136584004-G-T

14498195-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136584013-A-T

14498277-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136584092-G-T

14498282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136584097-T-C

14499584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136585045-A-G

14500014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136585269-G-A

14500018-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136585273-G-T

14500118-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136585350-A-T

14500176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136585422-G-A

14500376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136585616-A-G

14500734-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136585943-A-T

http://identifiers.org/hco/12/GRCh38#14500935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#136586150-C-A

14501027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136586238-C-T

14501037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136586248-T-C

http://identifiers.org/hco/12/GRCh38#14501046-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#136586257-A-C

14501357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136586494-A-G

14501680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136586789-A-G

14501686-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136586795-T-A

14501694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136586803-C-T

http://identifiers.org/hco/12/GRCh38#14501695-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#136586804-C-A

14501697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136586806-A-G

14501933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136586965-A-G

14502002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136587022-C-T

14502019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136587039-A-G

14502022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136587040-A-G

14502029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136587047-T-C

14502084-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136587095-G-C

14502084-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136587095-G-T

http://identifiers.org/hco/12/GRCh38#14502185-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#136587185-C-A

14502236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136587234-G-A

14502236-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136587234-G-T

14502412-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136587369-T-G

14502639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20092
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136587573-A-G