7500793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69057539-T-C

7500806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69057520-A-G

http://identifiers.org/hco/5/GRCh38#7501108-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#69057120-C-A

http://identifiers.org/hco/5/GRCh38#7503483-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#69056585-A-C

7503483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69056585-A-G

7503483-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69056585-A-T

7503675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69056426-C-T

http://identifiers.org/hco/5/GRCh38#7503769-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#69056348-C-A

7503783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69056334-C-T

7503811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69056306-T-C

http://identifiers.org/hco/5/GRCh38#7504249-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#69055583-C-A

7504254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69055578-G-A

7504370-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69055495-T-A

7504371-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69055494-C-G

7504482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69055381-T-C

7505203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69055290-T-C

7505215-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69055261-T-G

http://identifiers.org/hco/5/GRCh38#7505217-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#69055259-A-C

7505483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69055020-G-A

7505679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69054820-T-C

7506101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69054412-T-C

7506101-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69054412-T-G

7506318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69054185-A-G

7506611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69053872-C-T

7513961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69048932-A-G

7514328-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69048433-T-C

7514485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69048227-G-T

7514597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69048138-A-G

http://identifiers.org/hco/5/GRCh38#7514744-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#69041549-C-A

7514744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69041549-C-T

http://identifiers.org/hco/5/GRCh38#7514763-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#69041514-C-A

7514763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69041514-C-T

7515389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69040772-G-A

7515453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69040712-G-A

7515456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69040709-C-T

7515965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69040228-G-A

7516110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69040094-G-A

http://identifiers.org/hco/5/GRCh38#7516288-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#69039950-A-C

7516334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69039912-A-G

7516346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69039900-C-T

7516361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69039891-G-A

7516366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69039886-G-A

7516440-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69039820-G-C

7516710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69039576-C-T

http://identifiers.org/hco/5/GRCh38#7516833-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#69039458-C-A

7516833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69039458-C-T

7516850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69039440-G-A

7516850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69039440-G-T

7517127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69039212-G-A

7517160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69039190-A-G

7517161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69039189-G-A

7517350-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69039007-T-A

7517350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69039007-T-C

7517421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69038942-A-G

7517505-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69038864-C-G

7517571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69038807-G-A

7517595-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69038783-T-A

7517636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69038743-G-A

7517636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69038743-G-T

7518811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69038161-G-A

7518904-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69038069-G-T

7519059-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69037951-G-C

7519336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69037682-C-T

7519381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69037638-G-A

7519449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69037610-G-A

7519788-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69037270-G-T

7519846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69037204-C-T

7520116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69036978-G-A

7520208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69036888-G-A

7520579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69036364-T-C

7520587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69036356-T-C

7520633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69036318-G-A

7520633-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69036318-G-T

7520644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69036311-G-A

7520665-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69036290-T-A

7520665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69036290-T-C

7520691-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69036280-A-T

7520705-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69036266-G-C

7520807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 69036168-A-G

7520807-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 69036168-A-T

7520849-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 69036126-A-T

7520851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 69036124-C-T

7520856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 69036119-G-A

7520914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69036061-A-G

7520983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69036003-G-A

7520983-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69036003-G-T

7521050-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69035961-G-C

7521050-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69035961-G-T

7521083-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69035936-C-G

http://identifiers.org/hco/5/GRCh38#7521217-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#69035738-A-C

7521236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69035719-A-G

7523064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69033783-C-T

7523134-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69033726-G-C

7523206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69033678-G-A

7523238-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69033646-G-T

7523265-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69033626-C-G

7523265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69033626-C-T

http://identifiers.org/hco/5/GRCh38#7523293-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#69033600-C-A

7523293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69033600-C-T

7523579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69033332-C-T

7526664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69031159-A-G

7526712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69031112-C-T

7526769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69031062-A-G

7526769-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69031062-A-T

7526851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69030958-G-A

7526893-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69030920-A-T

7527070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69030746-T-C

7527354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69030503-A-G

7527417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69030440-A-G

http://identifiers.org/hco/5/GRCh38#7527735-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#69030121-C-A

7527742-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69030114-T-A

7528173-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69029699-G-T

7528310-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69029545-T-A

7528337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69029514-A-G

http://identifiers.org/hco/5/GRCh38#7528518-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#69029302-A-C

7528825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69028998-A-G

7529464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69028175-C-T

7529507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69028126-A-G

7530382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69026907-T-C

7530998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69026837-C-T

7531087-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69026759-T-G

7531125-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69026724-G-T

7531282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69026556-C-T

7531310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69026528-T-C

7531399-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69026445-C-G

7531520-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69026326-C-G

7531536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69026279-G-A

7531658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69026171-A-G

7532348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69025894-T-C

7532546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69025699-A-G

7532758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69025497-G-A

7532760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69025495-C-T

7532792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69025463-G-A

7532793-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69025462-G-T

7532818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69025431-G-A

7533441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69025000-A-G

7533492-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69024955-T-A

7533756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69024712-T-C

7534124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69024117-T-C

7534156-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69024056-C-G

7534218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69023991-T-C

7534253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69023957-G-A

7534383-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69023851-G-T

7534500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69023740-G-A

7534528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69023719-G-A

7534614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69023641-A-G

7534737-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69023539-C-G

7534781-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69023497-T-A

7534819-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69023455-C-G

7534872-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69023411-A-T

7534964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69023325-T-C

7534980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69023309-A-G

7535711-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69021821-G-T

7535716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69021816-G-A

7535879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69021660-C-T

7535884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69021655-T-C

7536100-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69021487-A-T

7536168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69021423-G-A

7536206-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69021397-C-G

7536224-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69021379-A-T

7536287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69021326-A-G

7536293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69021320-A-G

7536336-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69021291-C-G

7536336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69021291-C-T

7536488-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69021144-T-A

7536488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69021144-T-C

7536494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69021138-C-T

7537249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69020275-T-C

7537409-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69020137-G-C

7537437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69020109-A-G

7537503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69020080-C-T

7537781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69019825-G-A

7538167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69019417-T-C

7538206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69019377-C-T

http://identifiers.org/hco/5/GRCh38#7538225-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#69019359-A-C

7538493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69019074-T-C

7538497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69019070-T-C

7538541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69019026-A-G

7538728-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69018891-G-C

7538728-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69018891-G-T

7538792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69018826-G-A

7539104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69018716-C-T

7539488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69017747-T-C

7539515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69017728-C-T

7539539-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69017714-C-G

7539587-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69017666-G-T

7539707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69017547-A-G

7539740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69017518-C-T

7539759-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69017499-G-C

7539817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69017438-A-G

7539934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69017323-T-C

7540038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69017243-A-G

7540542-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69017026-C-G

7540984-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69016616-C-G

7541037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69016565-C-T

7541062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69016540-G-A

7541459-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69016141-G-C

7545529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69011318-G-A

7545529-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69011318-G-T

7545666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69011208-C-T

7545783-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69011091-T-G

7545796-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69011078-C-G

7545796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69011078-C-T

7545823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69011051-C-T

7545869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69011006-G-A

7545880-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69010995-G-C

7546118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69010780-C-T

7546130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69010768-G-A

7546160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69010737-T-C

7546263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69010633-G-A

7546333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69010569-T-C

7546475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69010432-G-A

7547086-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69010333-G-C

http://identifiers.org/hco/5/GRCh38#7547154-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#69010266-C-A

7547154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69010266-C-T

7547187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69010232-G-A

7547198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69010220-T-C

7547710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69009722-T-C

7548003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69009434-G-A

7548069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69009367-C-T

7548201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69009209-A-G

7548391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69008822-A-G

7548726-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69008488-A-T

7548751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69008463-T-C

7548855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69008360-A-G

7548857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69008358-G-A

7548913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69008305-A-G

7548920-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69008298-G-C

7548929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69008289-T-C

7548997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69008213-T-C

7549453-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69007797-T-G

http://identifiers.org/hco/5/GRCh38#7549529-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#69007727-C-A

7549529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69007727-C-T

7551487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69004311-A-G

7551489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69004309-G-A

7551508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69004290-A-G

7551739-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69004076-G-T

7551784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69004024-A-G

7551801-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69004007-T-A

http://identifiers.org/hco/5/GRCh38#7552303-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#69003557-C-A

7552510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69003049-G-A

http://identifiers.org/hco/5/GRCh38#7552593-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#69002966-A-C

7552795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69002471-T-C

7553681-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69001586-G-T

7554067-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69001208-A-T

7554250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69000690-A-G

7554333-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69000621-G-C

7554541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69000414-A-G

7554559-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69000395-T-G

7554615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69000341-C-T

7554965-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69000008-C-G

http://identifiers.org/hco/5/GRCh38#7555080-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68999914-A-C

7560581-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68999100-T-A

7560581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68999100-T-C

7560611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68999071-T-C

7564300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68997362-A-G

7564408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68997269-A-G

http://identifiers.org/hco/5/GRCh38#7564470-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68997219-C-A

7564470-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68997219-C-G

7564483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68997206-G-A

7564535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68997172-G-A

7564535-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68997172-G-C

7564553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68997156-C-T

7564576-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68997146-G-T

7564809-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68996903-C-G

7564869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68996854-G-A

7564869-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68996854-G-T

7564891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68996839-G-A

7564941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68996789-C-T

7565019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68996707-T-C

7565102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68996448-C-T

7565129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68996403-C-T

7565215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68996267-C-T

7565229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68996253-A-G

7565388-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68996100-T-A

7565388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68996100-T-C

7567255-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68994571-G-C

7567436-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68994408-C-G

7567466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68994378-G-A

7567525-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68994325-G-T

7567922-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68994023-C-G

7567991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68993981-T-C

7567995-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68993977-G-C

7567998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68993974-G-T

7568059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68993927-T-C

7568130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68993857-G-A

7568436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68993356-T-C

7568462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68993323-C-T

7568481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68993304-G-T

7568538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68993251-G-A

7568673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68993115-G-T

7570050-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68992207-A-T

7570075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68992239-A-G

7570075-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68992239-A-T

7570158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68992325-G-T

7570436-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68991788-G-C

7570606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68991630-G-A

7570738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68991535-A-G

http://identifiers.org/hco/5/GRCh38#7570779-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68991494-A-C

http://identifiers.org/hco/5/GRCh38#7570945-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68991340-C-A

7570957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68991328-G-A

7574674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68989239-C-T

http://identifiers.org/hco/5/GRCh38#7574675-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68989238-C-A

7574675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68989238-C-T

7574780-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68989152-A-T

7574916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68989014-C-T

7574962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68988965-T-C

7575341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68988764-C-T

7575998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68988067-A-G

7576018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68988048-T-C

7576176-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68987896-G-C

7576283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68987789-G-A

7576283-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68987789-G-C

7576419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68987524-G-A

7576579-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68987411-G-C

7576984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68987026-C-T

7577013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68986929-A-G

7577014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68986928-A-G

7577133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68986816-A-G

7577318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68986637-G-A

7577335-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68986620-G-C

http://identifiers.org/hco/5/GRCh38#7577341-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68986614-C-A

http://identifiers.org/hco/5/GRCh38#7577353-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68986602-A-C

7577486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68986471-A-G

7577517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68986446-A-G

7577520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68986443-G-A

http://identifiers.org/hco/5/GRCh38#7577804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68986214-C-A

7578270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68984203-G-T

7578581-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68983881-G-C

7586084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68979490-T-C

7586236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68979171-G-A

7586350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68979020-A-G

7586377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68978998-C-T

7586544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68978827-C-T

7586562-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68978810-G-T

7586631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68978736-G-A

7586655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68978712-G-A

7590242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68976791-A-G

7590951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68976160-G-A

7593411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68974773-C-T

7594610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68973591-G-A

7594930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68973272-A-G

7596130-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68971084-G-T

http://identifiers.org/hco/5/GRCh38#7596261-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68970933-C-A

7596261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68970933-C-T

7596332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68970870-A-G

7596379-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68970826-G-C

7596386-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68970819-T-A

7596386-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68970819-T-C

7596474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68970740-A-G

7596515-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68970713-T-G

7596574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68970651-T-C

7596855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68970393-T-C

7597045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68969831-G-A

7597045-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68969831-G-T

7597246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68969638-G-A

7597320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68969564-T-C

7597466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68969424-A-G

7598243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68968817-C-T

7598261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68968799-C-T

http://identifiers.org/hco/5/GRCh38#7598265-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68968795-A-C

7598376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68968670-A-G

7598422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68968634-A-G

7598457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68968599-C-T

7598506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68968553-T-C

7598606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68968465-T-C

http://identifiers.org/hco/5/GRCh38#7598756-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68968321-A-C

7598804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68968268-G-A

7598861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68968215-C-T

7598906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68968183-T-C

7600951-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68966665-T-G

7600973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68966643-T-C

7601282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68966382-T-C

http://identifiers.org/hco/5/GRCh38#7601327-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68966355-A-C

7601399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68966284-A-G

7601417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68966266-A-G

7601555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68966173-C-T

7602521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68964667-A-G

7602525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68964663-A-G

7602551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68964634-T-C

7602585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68964628-A-G

http://identifiers.org/hco/5/GRCh38#7602763-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68964453-A-C

http://identifiers.org/hco/5/GRCh38#7602935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68964296-C-A

7603037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68964198-T-C

7603256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68963982-G-A

7603500-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68963803-T-A

7603662-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68963652-G-C

7603663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68963651-A-G

7606400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68963493-A-G

7606413-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68963480-C-G

7606516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68963384-A-G

7606587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68963314-T-C

7606989-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 68962919-G-C

7607153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68962802-A-G

7607215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 68962734-C-T

7607218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 68962731-C-T

7607352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 68962598-C-T

http://identifiers.org/hco/5/GRCh38#7607438-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#68962513-A-C

7607510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68962443-A-G

7607520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68962433-C-T

7607615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68962342-C-T

7607630-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68962327-C-G

7607835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68962144-A-G

7608217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68961813-A-G

7609167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68960946-G-A

7609189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68960924-G-A

7610828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 68958191-A-G

7610924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68958101-A-G

7610935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68958090-A-G

7611164-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68957870-C-G

7611164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68957870-C-T

7611413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68957763-C-T

7611477-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68957689-G-T

7611563-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68957609-T-A

7612227-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68957316-G-C

7612263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68957281-T-C

7612451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68957111-G-A

7612706-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68956884-G-C

http://identifiers.org/hco/5/GRCh38#7615545-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68956123-C-A

7616012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68955618-G-A

7616013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68955617-T-C

7616056-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68955577-T-G

7616164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68955469-C-T

7616311-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68955353-C-G

7616406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68955265-T-C

7616696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68954914-A-G

7616800-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68954623-T-G

7616900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68954523-G-A

7616902-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68954511-T-C

7616965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68954450-A-G

7617782-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68953633-A-T

http://identifiers.org/hco/5/GRCh38#7617836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68953579-C-A

7617836-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68953579-C-G

7617882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68953531-A-G

7618164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68953253-G-A

7618873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68952899-T-C

7619242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68952585-T-C

7619297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68952533-G-A

7619371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68952460-G-A

7619443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68952395-T-C

7619582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68952212-A-G

7619762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68952070-T-C

7619771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68952057-C-T

7620460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68951442-G-A

7620507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68951395-T-C

http://identifiers.org/hco/5/GRCh38#7620511-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68951391-C-A

7620703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68951189-T-C

7620703-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68951189-T-G

7620728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68951162-A-G

7620766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68951130-G-A

http://identifiers.org/hco/5/GRCh38#7620843-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68951076-C-A

7620938-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68950991-T-A

7620938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68950991-T-C

7620958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68950971-C-T

7620991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68950935-T-C

7621002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68950924-T-C

http://identifiers.org/hco/5/GRCh38#7621053-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68950871-A-C

7621235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68950690-C-T

7621291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68950648-C-T

7621525-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68950419-G-T

7621612-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68950355-G-C

7621612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68950355-G-T

7621618-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68950349-T-G

http://identifiers.org/hco/5/GRCh38#7621931-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68950049-C-A

7622139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68949843-C-T

7622310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68949674-G-A

7623171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68948038-A-G

7623616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68947235-G-A

7623859-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68946998-G-C

7623930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68946926-A-G

7624162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68946652-A-G

http://identifiers.org/hco/5/GRCh38#7624326-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68946507-C-A

7624326-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68946507-C-G

7624484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68946377-G-A

http://identifiers.org/hco/5/GRCh38#7624722-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68946199-C-A

7624980-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68946002-G-C

7625009-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68945973-T-G

7625136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68945833-T-C

7625170-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68945798-T-G

7625174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68945794-C-T

7625274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68945687-A-G

7625320-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68945633-C-G

7625320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68945633-C-T

7625362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68945591-T-C

7625364-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68945589-G-C

7625450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68945509-G-A

7625940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68945038-G-A

http://identifiers.org/hco/5/GRCh38#7626089-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68944874-C-A

7626089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68944874-C-T

7626291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 68944672-A-G

http://identifiers.org/hco/5/GRCh38#7626343-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68944618-C-A

7626386-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68944576-T-C

7628738-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68941229-G-C

7628759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68941205-G-T

7629236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68940305-C-T

7629348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68940198-G-A

7629375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68940181-T-C

7629643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68939807-C-T

7629644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68939806-G-A

http://identifiers.org/hco/5/GRCh38#7631292-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68937028-A-C

7631430-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68936915-C-G

7631430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68936915-C-T

7631467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68936879-C-T

7631624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68936721-C-T

http://identifiers.org/hco/5/GRCh38#7631742-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68936604-A-C

7631742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68936604-A-G

7631835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68936515-T-C

7631926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68936284-C-T

7632116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68936083-A-G

7632202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68936006-C-T

7632290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68935911-C-T

7632402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68935819-C-T

7636453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68932570-G-A

7636453-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68932570-G-T

http://identifiers.org/hco/5/GRCh38#7636585-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68932447-A-C

http://identifiers.org/hco/5/GRCh38#7636753-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68932278-C-A

http://identifiers.org/hco/5/GRCh38#7637040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68931891-C-A

7637719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68931527-A-G

7639671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68931168-G-A

7639906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68930950-T-C

7640050-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68930810-C-G

http://identifiers.org/hco/5/GRCh38#7640054-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68930806-C-A

7640222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68930613-G-A

7640222-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68930613-G-C

7640684-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68930146-A-T

7640705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68930125-G-A

7640788-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68930043-G-C

7640791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68930037-G-A

7640825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68929998-G-A

7640825-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68929998-G-T

7640838-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68929985-A-T

7640903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68929943-A-G

7640919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68929927-T-C

http://identifiers.org/hco/5/GRCh38#7641040-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68929814-A-C

7641162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68929739-A-G

7641230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68929669-G-A

7644159-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68926132-T-A

http://identifiers.org/hco/5/GRCh38#7644352-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68925884-C-A

7644352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68925884-C-T

7644474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68925771-C-T

http://identifiers.org/hco/5/GRCh38#7644639-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68925593-C-A

7644648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68925584-G-A

7644648-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68925584-G-T

7644807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68925454-C-T

7645022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68925240-G-A

7645025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68925237-G-A

7645077-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68925185-C-G

7645501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68924653-A-G

7645592-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68924517-T-A

7646257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68923798-T-C

7646273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68923782-G-A

7646281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68923774-G-A

7646394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68923623-C-T

7646592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68923429-G-A

7646624-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68923396-G-T

7646637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68923383-T-C

7647825-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68923302-G-C

http://identifiers.org/hco/5/GRCh38#7648233-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68922918-A-C

7648233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68922918-A-G

7650327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68922573-A-G

7650353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68922547-A-G

http://identifiers.org/hco/5/GRCh38#7650729-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68922268-A-C

7650805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68922201-C-T

7650994-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68922012-A-T

7651055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68921965-C-T

http://identifiers.org/hco/5/GRCh38#7651065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68921955-C-A

7652145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68921738-C-T

7652148-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68921735-T-G

7652509-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68921396-G-C

7653041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68920684-G-A

http://identifiers.org/hco/5/GRCh38#7653063-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68920667-C-A

7653852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68920168-C-T

7654014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68919990-G-A

http://identifiers.org/hco/5/GRCh38#7654026-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68919981-C-A

7654026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68919981-C-T

7654083-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68919925-C-G

7654083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68919925-C-T

7654087-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68919921-G-C

7654183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68919855-G-A

7654183-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68919855-G-C

7654323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68919747-G-A

7654323-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68919747-G-T

7654427-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68919636-G-C

7654483-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68919579-G-T

7654549-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68919505-T-G

7654744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68918904-A-G

7655272-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68918457-T-A

7656552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68916982-T-C

7656834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68916764-T-C

7657452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68916285-C-T

http://identifiers.org/hco/5/GRCh38#7657473-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68916264-A-C

7657473-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68916264-A-T

7657504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68916224-G-T

7657846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68915922-A-G

7657895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68915872-A-G

7657922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68915842-G-A

7657922-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68915842-G-T

7658053-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 68915709-T-A

7658053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 68915709-T-C

7658092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 68915675-C-T

7658769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68915446-C-T

7658824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68915404-G-A

7659415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68914359-T-C

7662302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68908326-G-A

7662317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68908311-T-C

7662423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68908213-G-A

7662423-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68908213-G-C

7662640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68907959-A-G

7662726-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68907869-T-A

7662863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68907727-C-T

7662903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68907685-A-G

7662924-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68907664-C-G

7662924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68907664-C-T

7663088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68907527-A-G

7663557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68907047-G-A

7663702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68906934-C-T

7663736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68906900-A-G

http://identifiers.org/hco/5/GRCh38#7663882-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68906713-A-C

7663922-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68906672-T-A

7664165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68906480-G-A

7664302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68906341-A-G

7664332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68906311-G-A

7664429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68906250-A-G

7665281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68906156-C-T

http://identifiers.org/hco/5/GRCh38#7665347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68906098-C-A

http://identifiers.org/hco/5/GRCh38#7665423-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68906021-C-A

7665481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68905949-A-G

7665532-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68905877-G-C

http://identifiers.org/hco/5/GRCh38#7666668-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68905286-C-A

7666852-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68905091-C-G

7666852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68905091-C-T

7667006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68904971-G-A

7667006-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68904971-G-C

7667006-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68904971-G-T

7667112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68904870-G-A

7667250-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68904731-T-A

7667372-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68904623-A-T

7668652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68903304-A-G

7669007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68902977-C-T

7669050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68902940-G-A

7669269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68902734-G-A

7669269-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68902734-G-T

7669273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68902730-G-A

7669441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68902612-G-A

7669446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68902607-A-G

7669572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68902522-C-T

7671302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68901183-G-A

7671392-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68901092-G-T

7671431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68901055-C-T

7671593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68900885-A-G

7671740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68900740-G-A

7674188-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68899804-T-G

7674434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68899574-G-A

7674503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68899506-C-T

7674570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68899426-T-C

7674626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68899370-A-G

7674634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68899362-T-C

7675319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68899123-T-C

7675474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68899005-G-A

http://identifiers.org/hco/5/GRCh38#7675534-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68898948-C-A

7675591-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68898889-C-G

7675595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68898885-C-T

7675618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68898857-T-C

7676620-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68898677-T-G

7676638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68898594-T-C

7676666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68898560-G-A

7677338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68898262-G-A

7677416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68898188-G-A

7677416-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68898188-G-C

7677416-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68898188-G-T

7677418-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68898179-T-C

7677562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68898039-C-T

7677661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68897937-G-A

7678074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68897545-T-C

7678324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68897302-A-G

7678524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68897101-G-A

7678683-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68896941-C-G

7678737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68896898-C-T

7678820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68896803-T-C

7678867-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68896758-T-A

7679010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68896622-G-A

7679293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68896027-G-T

7679335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68895994-A-G

7680642-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68895216-G-C

7680738-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68895130-A-T

7680874-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68894984-G-T

7680875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68894983-G-A

7680993-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68894888-G-T

7681241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68894604-T-C

7681241-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68894604-T-G

7681244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68894600-T-C

7681314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68894545-G-A

7681352-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68894513-C-G

7681354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68894511-G-A

7681526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68894276-A-G

7681652-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68894077-G-C

7681652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68894077-G-T

7681859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68893870-C-T

7681904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68893831-C-T

7682048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68893739-C-T

7682132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68893654-A-G

7682132-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68893654-A-T

7682200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68893587-G-A

7682937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68892175-C-T

7682975-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68892145-A-G

7683120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68892076-A-G

7683231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68891981-A-G

7683287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68891919-C-T

http://identifiers.org/hco/5/GRCh38#7683297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68891910-C-A

7683297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68891910-C-T

7683342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68891871-A-G

7683358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68891855-A-G

7683606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68891477-G-A

7683698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68891217-C-T

7683980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68890960-T-C

7684067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68890883-G-A

7684768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68890262-G-A

7684768-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68890262-G-T

7684970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68890081-A-G

7684970-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68890081-A-T

7684974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68890077-T-C

7685065-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68889932-C-G

7685078-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68889922-A-T

7685088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68889912-G-A

7685088-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68889912-G-T

7685281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 68889714-T-C

7685295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68889700-G-A

7685295-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68889700-G-T

7685335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68889660-A-G

7685491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68889516-T-C

7685577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68889423-G-A

7685588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68889412-T-C

http://identifiers.org/hco/5/GRCh38#7685790-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68889203-C-A

7685846-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68889107-G-T

7685859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68889097-T-C

7685859-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68889097-T-G

7686023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68888935-A-G

7687073-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68888410-A-T

7687201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68888283-A-G

7687260-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68888223-G-C

7687429-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68888095-A-T

7687433-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68888091-G-T

7689888-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68887575-G-C

http://identifiers.org/hco/5/GRCh38#7689929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68887534-C-A

7690078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68887362-C-T

7690156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68887316-C-T

7690309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68887165-A-G

http://identifiers.org/hco/5/GRCh38#7690446-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68887019-C-A

http://identifiers.org/hco/5/GRCh38#7690468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68886998-C-A

7690468-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68886998-C-G

http://identifiers.org/hco/5/GRCh38#7690565-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68886899-A-C

7690569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 68886894-T-C

7690664-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 68886837-T-A

7690664-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 68886837-T-G

7690667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 68886834-T-C

http://identifiers.org/hco/5/GRCh38#7690673-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68886828-C-A

7690673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 68886828-C-T

http://identifiers.org/hco/5/GRCh38#7690707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68886797-C-A

7690710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 68886794-T-C

7690724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 68886780-A-G

7690754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 68886750-C-T

7690760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 68886744-C-T

http://identifiers.org/hco/5/GRCh38#7690911-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68886606-A-C

http://identifiers.org/hco/5/GRCh38#7690917-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68886600-C-A

7691055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 68886499-T-C

7691061-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 68886493-G-T

7691082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 68886478-G-A

7691082-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 68886478-G-T

http://identifiers.org/hco/5/GRCh38#7691090-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68886470-A-C

7691090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 68886470-A-G

7691112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 68886452-G-A

7691112-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 68886452-G-T

7691120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 68886445-G-A

7691120-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 68886445-G-C

7691120-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 68886445-G-T

http://identifiers.org/hco/5/GRCh38#7691157-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68886407-C-A

7691157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 68886407-C-T

7691159-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 68886405-G-T

7691199-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 68886365-G-T

7691236-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 68886327-G-T

7691492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 68886094-A-G

http://identifiers.org/hco/5/GRCh38#7691511-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68886077-C-A

7691710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 68885918-T-C

7692368-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68885486-A-T

7692401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68885482-A-G

7692416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68885467-G-A

7692443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68885444-A-G

7695559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68883041-G-A

7695667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68882934-G-T

7695924-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68882681-T-A

7695924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68882681-T-C

7696171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68882502-G-A

7696199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68882466-A-G

7696334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68882362-T-C

7696515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68882195-A-G

7696625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68882094-T-C

7696750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68881997-G-A

7697870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68880679-T-C

7697920-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68880624-C-G

7698017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68880542-C-T

7698067-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68880491-A-T

7698123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68880439-T-C

7698148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68880413-G-A

7698157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68880407-G-T

7698380-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68880188-T-A

7706122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68879416-A-G

7706236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68878983-G-A

http://identifiers.org/hco/5/GRCh38#7706607-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68878649-C-A

7706607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68878649-C-T

7706629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68878627-G-A

http://identifiers.org/hco/5/GRCh38#7706781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68878476-C-A

7706781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: missense variant
orthologous variants: 68878476-C-T

7707002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68878256-T-C

http://identifiers.org/hco/5/GRCh38#7707010-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68878248-C-A

7707010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68878248-C-T

7707053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68878210-A-G

7707053-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68878210-A-T

7707145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68878013-T-C

7707163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68877995-A-G

7707188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68877973-G-A

7707314-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68877847-T-G

7707407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68877757-A-G

7707415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68877749-C-T

7707560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68877612-T-C

7707561-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68877611-G-C

7707561-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68877611-G-T

7707666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68877487-C-T

7707861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 68877301-T-C

http://identifiers.org/hco/5/GRCh38#7707883-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68877262-C-A

7707892-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 68877252-G-T

7707956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 68877190-A-G

7708076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 68877058-A-G

7708093-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 68877031-G-T

7708256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68876895-A-G

7708256-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68876895-A-T

7708518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68876636-G-A

7708763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68876399-C-T

7708824-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68876367-G-T

7708880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68876316-A-G

7708906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68876294-A-G

7709125-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68876134-G-T

7709203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 68876093-A-G

http://identifiers.org/hco/5/GRCh38#7709428-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68875874-A-C

7709428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68875874-A-G

http://identifiers.org/hco/5/GRCh38#7709460-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68875837-C-A

7709460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68875837-C-T

7709461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68875836-T-C

7709483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68875814-T-C

7709736-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68875707-A-T

7709918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68875546-T-C

7709979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68875483-G-A

7712716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68872565-T-C

7712836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68872444-A-G

7712836-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68872444-A-T

7712908-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68872372-T-A

7712978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68872298-T-C

7712978-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68872298-T-G

7713318-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68871949-A-T

7713791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68871654-A-G

7714202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68871277-C-T

7714212-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68871267-G-T

http://identifiers.org/hco/5/GRCh38#7714325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#68871189-C-A

7714335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68871179-A-G

7714354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68871169-C-T

7714365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68871158-G-A

7714365-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68871158-G-T

7714806-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68870756-T-G

7714941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68870625-C-T

7715036-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68870542-A-T

7715187-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68870400-T-A

7715443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68870145-A-G

7715462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68870128-T-C

7715624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68869922-A-G

7715628-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68869918-C-G

7716074-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68869479-C-G

7716124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68869421-A-G

7716144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68869400-A-G

http://identifiers.org/hco/5/GRCh38#7717132-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68868922-C-A

7717269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68868786-A-G

7717318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68868629-A-G

7717395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68868568-T-C

7717445-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68868523-C-G

7717993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68867722-G-A

7717993-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68867722-G-C

7719271-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68866069-C-G

7719798-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68865605-C-G

7719867-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68865534-G-C

7720035-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68865352-T-A

7720035-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68865352-T-G

7720104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68865286-A-G

7720137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68865260-A-G

7720145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68865252-C-T

http://identifiers.org/hco/5/GRCh38#7720168-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68865191-C-A

7720254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68865058-A-G

7720273-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68865040-T-G

7722292-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68864630-T-A

7722330-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68864600-C-G

7722335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68864595-T-C

7722359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68864566-T-C

7722473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68864445-A-G

7722473-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68864445-A-T

7723508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68862223-C-T

7723518-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68862213-T-G

7723588-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68862148-T-A

7724429-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68861359-T-A

7724451-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68861333-T-A

7724451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68861333-T-C

http://identifiers.org/hco/5/GRCh38#7724639-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68861148-C-A

7724639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68861148-C-T

7724653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68861137-T-C

7724654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68861136-C-T

http://identifiers.org/hco/5/GRCh38#7724732-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68860971-A-C

7724732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68860971-A-G

7724732-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68860971-A-T

http://identifiers.org/hco/5/GRCh38#7724761-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68860937-C-A

7724761-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68860937-C-G

7724761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68860937-C-T

7725264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68860316-A-G

7725362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68860216-A-G

7725362-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68860216-A-T

7725405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68860172-A-G

7725574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68859743-C-T

7725631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68859667-A-G

7725632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68859666-G-A

7725717-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68859589-C-G

7725717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68859589-C-T

7725720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68859586-G-A

7725848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68859457-A-G

7725881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68859421-A-G

7726005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68859305-G-T

http://identifiers.org/hco/5/GRCh38#7726032-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68859276-A-C

7726085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68859218-C-T

7726143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68859158-G-A

7726787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68858561-T-C

7727109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68858267-T-C

http://identifiers.org/hco/5/GRCh38#7727114-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68858262-A-C

7727122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68858254-T-C

7727209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 68858162-G-A

7727209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 68858162-G-T

7727321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68858048-G-T

7727332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68858037-A-G

7727700-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68857275-G-T

7727752-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68857237-G-T

7727822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68857172-C-T

7728559-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68855555-A-T

http://identifiers.org/hco/5/GRCh38#7728979-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68847591-C-A

7729104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68847459-T-C

http://identifiers.org/hco/5/GRCh38#7729158-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68847389-C-A

7729329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68847237-T-C

7729331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68847235-G-A

7729331-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68847235-G-C

7729460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68847124-T-C

http://identifiers.org/hco/5/GRCh38#7729499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68847100-C-A

7729590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68847029-G-T

7732080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68846508-G-A

7732370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68846258-G-A

7732388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68846240-G-A

7732388-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68846240-G-C

7732515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68846116-C-T

http://identifiers.org/hco/5/GRCh38#7732610-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68845963-A-C

7732686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68845790-C-T

7733131-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68845351-G-C

7733132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68845350-C-T

7734276-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68844229-T-A

7734283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68844222-T-C

7734659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68843856-C-T

7743195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68837917-T-C

7743226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68837886-C-T

7743291-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68837827-C-G

7743305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68837812-G-A

7743305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68837812-G-T

http://identifiers.org/hco/5/GRCh38#7743314-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68837803-A-C

7743558-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68837571-T-A

7743582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68837547-T-C

7743729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 68837401-G-A

7743729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 68837401-G-T

7743803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68837326-A-G

7743841-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68837292-T-G

7743920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68837219-A-G

7744068-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68836935-G-C

7744413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68836707-C-T

7744602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68836500-G-A

7744617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68836485-A-G

7745984-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68836080-T-A

7746097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68835949-G-A

7746097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68835949-G-T

7746230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 68835827-G-T

7746240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 68835820-G-A

7746240-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 68835820-G-T

7746301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 68834263-G-A

7746301-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 68834263-G-T

7746307-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 68834257-G-T

7746459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68834143-G-A

7746492-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68834112-C-G

http://identifiers.org/hco/5/GRCh38#7746498-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68834106-A-C

7746827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68833799-G-A

http://identifiers.org/hco/5/GRCh38#7749529-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68832394-A-C

7749692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68832207-T-C

7749734-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 68832170-T-A

7749763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 68832141-T-C

7749775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68832129-A-G

7749796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68832105-G-A

7749835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68832066-A-G

7749835-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68832066-A-T

7749854-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68832044-G-C

7749854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68832044-G-T

7749886-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68832014-G-T

7749887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68832013-T-C

7749925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68831971-C-T

7749955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68831949-T-C

7750016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68831894-A-G

7750085-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68831820-T-A

7750097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68831808-G-A

7750101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68831804-A-G

7750119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68831776-G-A

7750170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68831704-T-C

7750185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68831689-C-T

7750202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68831672-T-C

7750206-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68831668-G-T

7750216-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68831664-G-C

7750248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68831619-G-A

7750264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68831603-G-A

7750399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68831467-C-T

7750463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68831406-G-A

7750472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68831397-A-G

7750474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68831395-A-G

7750506-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68831369-C-G

7750514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68831361-C-T

7750578-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68831311-T-G

7750675-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68831210-G-T

7750676-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68831209-A-T

7750732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68831161-T-C

7753224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68830616-A-G

7753534-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68830373-T-G

7754629-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68829505-G-T

http://identifiers.org/hco/5/GRCh38#7755278-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68829147-A-C

7755278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68829147-A-G

http://identifiers.org/hco/5/GRCh38#7755334-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68829091-C-A

7755334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68829091-C-T

7755398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68829046-G-A

7755603-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68828854-A-T

7755618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68828839-G-A

7755861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68828634-A-G

7756393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68828184-T-C

7756419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68828161-G-A

7756419-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68828161-G-T

7756674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68827904-G-A

7756677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68827901-G-A

7756922-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68827220-A-T

7756971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68827182-C-T

7757273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68826894-A-G

7757412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68826766-T-C

7757420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68826758-C-T

7757426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68826755-T-C

7760881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68825334-C-T

7761046-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68825186-T-G

7761118-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68825134-T-G

7761479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68825100-A-G

7761479-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68825100-A-T

7761503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68825063-G-A

7761535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68825018-G-T

http://identifiers.org/hco/5/GRCh38#7761538-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68825013-C-A

7761538-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68825013-C-G

7761686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68824849-G-T

7761821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68824718-A-G

7762063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68824499-T-C

7762195-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68824386-T-G

7762226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68824357-G-A

7762226-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68824357-G-T

7762534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68824074-G-A

7762648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68823959-T-C

7762867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68823830-G-A

7763044-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68823691-T-G

7763059-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68823676-G-T

7763063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68823672-G-T

7763086-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68823650-T-A

7763125-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68823609-G-T

7763132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68823602-C-T

http://identifiers.org/hco/5/GRCh38#7763310-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68823521-C-A

7763318-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68823513-C-G

http://identifiers.org/hco/5/GRCh38#7763457-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68823334-A-C

7763651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68823210-C-T

http://identifiers.org/hco/5/GRCh38#7763901-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68822944-C-A

7764072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68822698-T-C

7764150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68822623-C-T

7764162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68822605-A-G

7764452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68822325-G-A

7764452-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68822325-G-C

7764496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68822287-A-G

7764497-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68822286-T-A

7765144-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68821600-T-G

7765157-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68821588-T-G

http://identifiers.org/hco/5/GRCh38#7765392-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68821345-A-C

7765550-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68821206-C-G

http://identifiers.org/hco/5/GRCh38#7766109-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68820760-C-A

http://identifiers.org/hco/5/GRCh38#7766576-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68820248-C-A

7766576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68820248-C-T

http://identifiers.org/hco/5/GRCh38#7766593-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68820227-C-A

7766634-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68820185-A-T

7766720-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: missense variant
orthologous variants: 68820096-C-G

7766759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: missense variant
orthologous variants: 68820057-A-G

7766771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: missense variant
orthologous variants: 68820045-G-A

http://identifiers.org/hco/5/GRCh38#7766868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68819951-C-A

7766868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68819951-C-T

http://identifiers.org/hco/5/GRCh38#7766876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68819943-C-A

7766876-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68819943-C-G

7766876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68819943-C-T

7766879-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68819940-T-G

7770649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68818445-T-C

7770748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68818348-A-G

7771122-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68817967-A-T

7771225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68817892-G-A

7771417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68817716-G-A

7771509-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68817630-T-G

7771594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68817540-T-C

7772011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68817222-C-T

7772758-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68816927-A-T

7772820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68816865-G-T

7772879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68816808-G-A

7772879-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68816808-G-T

7772901-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron variant
orthologous variants: 68816790-A-T

7772974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: missense variant
orthologous variants: 68816714-G-A

7773111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68816575-G-A

http://identifiers.org/hco/5/GRCh38#7773120-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68816566-C-A

7773158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68816524-A-G

http://identifiers.org/hco/5/GRCh38#7773211-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68816476-C-A

http://identifiers.org/hco/5/GRCh38#7773215-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68816472-C-A

7773215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68816472-C-T

http://identifiers.org/hco/5/GRCh38#7773233-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68816456-A-C

7773440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68816138-G-A

7773449-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68816038-G-T

7773454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68815996-G-A

7773596-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68815838-T-A

7773596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68815838-T-C

7773597-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68815837-T-A

7773800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68815633-A-G

7773851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68815547-T-C

7773892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68815515-A-G

7774123-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68815222-T-G

7774278-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68815081-G-T

7774407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68814937-A-G

7774596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68814751-G-A

7774631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68814716-G-A

7776356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68814046-G-A

7776398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68814008-C-T

7777413-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68813472-A-T

http://identifiers.org/hco/5/GRCh38#7777605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68813331-C-A

7777605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68813331-C-T

7777756-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68813116-G-T

7777879-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68812996-T-A

7777922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68812964-A-G

7778061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68812833-T-C

7778115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68812763-G-A

http://identifiers.org/hco/5/GRCh38#7778242-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68812646-C-A

7778242-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68812646-C-G

7778242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68812646-C-T

7778338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68812561-A-G

http://identifiers.org/hco/5/GRCh38#7778397-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68812502-C-A

7778464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68812443-G-A

7778510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68812397-A-G

7778551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68812367-G-A

7778673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68812247-T-C

http://identifiers.org/hco/5/GRCh38#7778744-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68812176-C-A

7778744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68812176-C-T

7779084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68811859-T-C

7779367-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68811659-G-T

7779371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68811654-A-G

7779409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68811620-C-T

http://identifiers.org/hco/5/GRCh38#7779436-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68811593-C-A

7779436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68811593-C-T

7779951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68811268-G-A

7780109-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68811098-T-A

7780109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68811098-T-C

7780178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68811034-C-T

7780207-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68811013-G-T

7780802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68809125-A-G

7780934-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68808994-C-G

http://identifiers.org/hco/5/GRCh38#7781014-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68808905-A-C

7781211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68808676-G-A

7781350-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68808514-G-T

7781531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68808324-G-A

http://identifiers.org/hco/5/GRCh38#7781535-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68808320-A-C

7781535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68808320-A-G

7781603-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68808257-C-G

7781682-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68808219-C-G

7781682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68808219-C-T

7781689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68808212-T-C

7781778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68808120-T-C

7781778-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68808120-T-G

7781808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68808113-A-G

7781811-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68808110-C-G

7782064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68807881-A-G

http://identifiers.org/hco/5/GRCh38#7782116-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68807830-C-A

7782116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68807830-C-T

http://identifiers.org/hco/5/GRCh38#7782118-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68807828-C-A

7782118-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68807828-C-G

7782118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68807828-C-T

http://identifiers.org/hco/5/GRCh38#7782238-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68807711-C-A

7782243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 68807704-G-A

http://identifiers.org/hco/5/GRCh38#7782343-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68807601-C-A

7782361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68807583-T-C

7782473-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68807497-G-T

7782791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68807194-A-G

7782867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68807131-T-C

7783017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68806996-G-A

7783174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68806796-C-T

7783282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68806713-G-A

7783289-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68806706-A-G

7783291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68806704-G-A

7783310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68806685-G-A

7783310-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68806685-G-T

7783333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68806651-G-A

7783394-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68806520-T-G

7783676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68806281-A-G

7783730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68806237-A-G

7783934-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68806043-G-C

7784018-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68805947-C-G

7784238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68805713-T-C

7784250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68805701-A-G

7784250-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68805701-A-T

http://identifiers.org/hco/5/GRCh38#7784541-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68805430-A-C

7784598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68805367-A-G

7784761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68805220-C-T

7784792-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68805202-C-G

7784803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68805191-G-T

7785191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68804820-A-G

7785388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68804651-G-A

7785467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68804577-C-T

7785509-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68804539-G-T

7785526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68804522-G-A

7785598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68804441-A-G

7785679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68804361-G-A

7785679-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68804361-G-T

7785919-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68804101-C-G

7785919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68804101-C-T

7785995-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68804038-C-G

7786049-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68803990-T-G

7786668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68803297-T-C

7786732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68803217-C-T

7787135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68802934-G-A

7787135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68802934-G-T

7787310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68802751-G-A

7787655-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68802395-G-T

http://identifiers.org/hco/5/GRCh38#7787917-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68801196-C-A

7787936-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68801176-T-G

7788010-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68801100-C-G

7788010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68801100-C-T

7788016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68801094-A-G

7788102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68800999-T-C

7788149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68800951-C-T

7789012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68800841-T-C

7789037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68800816-A-G

http://identifiers.org/hco/5/GRCh38#7789523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68800259-C-A

7789523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68800259-C-T

7789583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68800200-C-T

7790181-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68798929-G-T

http://identifiers.org/hco/5/GRCh38#7790294-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68798818-A-C

7790435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68798221-T-C

7790508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68798141-G-A

7790534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68798108-C-T

http://identifiers.org/hco/5/GRCh38#7796271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68796202-C-A

7796273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68796200-G-A

7796273-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68796200-G-T

7796284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68796189-C-T

http://identifiers.org/hco/5/GRCh38#7796721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68795800-C-A

7796721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68795800-C-T

http://identifiers.org/hco/5/GRCh38#7796793-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68795760-C-A

7796793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68795760-C-T

7796794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68795759-T-C

7796844-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68795733-G-T

7796906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68795672-C-T

7797051-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68795576-G-C

7797051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68795576-G-T

7797057-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68795570-A-T

http://identifiers.org/hco/5/GRCh38#7797310-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68795352-C-A

7797429-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68795269-C-G

7797429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68795269-C-T

http://identifiers.org/hco/5/GRCh38#7797644-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68795078-C-A

7797656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68795066-T-C

7797908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68794777-T-C

http://identifiers.org/hco/5/GRCh38#7798170-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68794567-C-A

7798170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68794567-C-T

7798171-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68794566-T-A

7798171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68794566-T-C

7798171-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68794566-T-G

7798201-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68794528-A-T

7798206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68794523-G-A

7798206-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68794523-G-T

7798221-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68794502-T-A

7798221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68794502-T-C

7798221-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68794502-T-G

7798259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68794471-A-G

http://identifiers.org/hco/5/GRCh38#7798401-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68794364-C-A

7798401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68794364-C-T

7798907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68794191-A-G

http://identifiers.org/hco/5/GRCh38#7798961-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68794137-A-C

7798988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68794109-A-G

7799010-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68794090-G-C

7799169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68793976-T-C

7799172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68793973-G-A

7799172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68793973-G-T

7799174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68793971-C-T

7799195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68793952-T-C

7799199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68793948-A-G

7799228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68793919-T-C

7799251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68793896-G-T

7799299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68793846-T-C

http://identifiers.org/hco/5/GRCh38#7799447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68793708-C-A

7799538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68793627-G-A

7799538-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68793627-G-T

7799593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68793573-G-A

7799614-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68793552-G-T

7799696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68793422-T-C

7799698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68793420-A-G

7799698-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68793420-A-T

7799738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68793327-A-G

7799739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68793326-A-G

7799740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68793325-A-G

7799931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68793137-T-C

http://identifiers.org/hco/5/GRCh38#7799950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68793119-C-A

7799958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68793111-G-A

7799958-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68793111-G-T

7800021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68793057-G-A

7800021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68793057-G-T

7800071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68793005-A-G

http://identifiers.org/hco/5/GRCh38#7800081-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68792995-C-A

7800081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68792995-C-T

7800226-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68792883-G-C

7800229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68792880-T-C

7800229-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68792880-T-G

7800239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68792870-T-C

7800263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68792846-G-A

7800263-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68792846-G-T

7800285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68792825-T-C

7800345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68792773-A-G

7800359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68792759-C-T

http://identifiers.org/hco/5/GRCh38#7800865-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68792598-C-A

7800865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68792598-C-T

7800896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68792564-G-A

7800896-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68792564-G-T

7800931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68792540-C-T

7800944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68792527-A-G

http://identifiers.org/hco/5/GRCh38#7800950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68792521-C-A

7801058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68792408-A-G

http://identifiers.org/hco/5/GRCh38#7801107-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68792360-C-A

7801107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68792360-C-T

7801112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68792356-T-C

7801127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68792341-A-G

7801127-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68792341-A-T

7801160-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68792318-G-T

http://identifiers.org/hco/5/GRCh38#7801201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68792279-C-A

7801228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68792248-G-A

7801266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68792211-T-C

http://identifiers.org/hco/5/GRCh38#7801289-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68792189-C-A

7801289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68792189-C-T

http://identifiers.org/hco/5/GRCh38#7801388-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68792096-C-A

7801388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68792096-C-T

http://identifiers.org/hco/5/GRCh38#7801416-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68792068-C-A

7801494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68792027-T-C

7801497-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68792024-G-T

http://identifiers.org/hco/5/GRCh38#7801539-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68791991-C-A

7801539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68791991-C-T

7801597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68791942-T-C

7801604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68791935-A-G

7801641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68791901-G-T

7801674-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68791868-G-T

7801721-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68791822-T-A

7801721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68791822-T-C

7801825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68791214-T-C

7801826-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68791213-C-G

7801826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68791213-C-T

7801840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68791199-A-G

http://identifiers.org/hco/5/GRCh38#7801844-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68791195-C-A

7801844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68791195-C-T

http://identifiers.org/hco/5/GRCh38#7801896-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68791142-C-A

7801896-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68791142-C-G

7801896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68791142-C-T

7801920-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68791118-T-A

7801920-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68791118-T-G

http://identifiers.org/hco/5/GRCh38#7802082-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68790888-C-A

7802082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68790888-C-T

7802087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68790883-G-A

7802087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68790883-G-T

7802105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68790858-G-A

7802105-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68790858-G-C

7802105-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68790858-G-T

7802168-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68790765-G-T

7802175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68790758-G-A

7802175-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68790758-G-T

7802221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 68790717-C-T

7802422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68790511-A-G

http://identifiers.org/hco/5/GRCh38#7802447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68790486-C-A

7802447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68790486-C-T

http://identifiers.org/hco/5/GRCh38#7802493-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68790443-C-A

7802694-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68790258-A-T

7802972-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68789956-G-T

7802981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68789947-A-G

7802993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68789935-A-G

7803045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68789882-G-A

7803155-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 68789785-T-A

7803155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 68789785-T-C

7803250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68789684-A-G

7803284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68789650-A-G

7803441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68789504-G-A

7804101-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68789389-T-G

7804110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68789380-G-A

7804127-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68789353-T-G

7804129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68789351-G-A

http://identifiers.org/hco/5/GRCh38#7804315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68789182-C-A

7804315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68789182-C-T

7804403-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68789099-G-T

7804441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68789062-A-G

http://identifiers.org/hco/5/GRCh38#7804443-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68789060-C-A

7804443-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68789060-C-G

7804443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68789060-C-T

7804497-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68789021-G-T

7804675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 68788844-A-G

http://identifiers.org/hco/5/GRCh38#7804715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68788799-C-A

7804715-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68788799-C-G

7804715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68788799-C-T

7804717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68788797-G-A

http://identifiers.org/hco/5/GRCh38#7804749-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68788774-A-C

7804789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68788735-T-C

7804797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68788727-G-A

7804797-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68788727-G-C

7804797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68788727-G-T

7804806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68788718-A-G

7805893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68787169-T-C

7806003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68787067-G-A

7806043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68787028-A-G

7806077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68787007-A-G

7806119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68786961-T-C

7806120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68786960-T-C

7806403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68786685-C-T

7808565-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68786522-C-G

http://identifiers.org/hco/5/GRCh38#7808636-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68786430-C-A

http://identifiers.org/hco/5/GRCh38#7808655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68786416-C-A

7808930-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68786163-G-C

7809080-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68786050-T-A

7809151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68785993-G-A

7809151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68785993-G-T

7809235-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68785913-T-G

7809843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68785348-C-T

7810022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68785153-C-T

7811051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68784671-T-C

7811135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68784599-G-A

7811135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68784599-G-T

7811568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68784490-A-G

7811571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68784487-T-C

http://identifiers.org/hco/5/GRCh38#7811633-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68784431-C-A

7811633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68784431-C-T

7811675-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68784386-T-A

7811789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68784261-A-G

7811957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68784078-G-A

7811962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68784073-T-C

7812182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68783871-G-A

7812182-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68783871-G-T

7812286-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68783779-G-C

http://identifiers.org/hco/5/GRCh38#7812476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68783585-C-A

7813026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68782413-T-C

7813036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68782403-C-T

7813410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68782055-T-C

7813788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68781695-C-T

7813873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68781621-A-G

http://identifiers.org/hco/5/GRCh38#7813982-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68781517-C-A

7814058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68781451-G-A

7814477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68780469-G-A

7814477-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68780469-G-T

7814570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68780393-C-T

7814633-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68780329-A-G

http://identifiers.org/hco/5/GRCh38#7814638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68780324-C-A

7814731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68780246-A-G

7816017-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 68779853-T-A

7816149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 68779729-G-A

7816232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 68779662-G-A

7816250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 68779644-A-G

http://identifiers.org/hco/5/GRCh38#7816283-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68779614-A-C

7816285-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68779612-C-G

7816493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68779462-G-A

7816617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 68779367-C-T

7816639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 68779342-G-A

http://identifiers.org/hco/5/GRCh38#7816705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#68779270-C-A

http://identifiers.org/hco/5/GRCh38#7816786-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#68779216-A-C

7816994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68779013-A-G

7817535-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68778314-A-T

7818122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68777751-A-G

7818233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68777620-G-A

7819567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68776296-A-G

7819620-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68776256-A-T

7819919-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68775966-C-G

7819973-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68775916-C-G

http://identifiers.org/hco/5/GRCh38#7819991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68775898-C-A

7819991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68775898-C-T

7820176-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68775728-C-G

7820176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68775728-C-T

http://identifiers.org/hco/5/GRCh38#7820726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68773879-C-A

http://identifiers.org/hco/5/GRCh38#7820786-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68773809-A-C

7820897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68773702-A-G

7820904-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68773696-T-G

7820925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68773671-T-C

7820929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68773667-G-A

7821519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68773015-C-T

7826678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68769025-T-C

7827364-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 68768339-C-G

7827419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 68768285-G-A

7827419-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 68768285-G-C

7827419-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 68768285-G-T

7827514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 68768190-A-G

7827569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: 3 prime UTR variant
orthologous variants: 68768119-T-C

7827675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: 3 prime UTR variant
orthologous variants: 68768021-T-C

7827735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: 3 prime UTR variant
orthologous variants: 68767962-C-T

7827744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: 3 prime UTR variant
orthologous variants: 68767953-T-C

7827758-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: 3 prime UTR variant
orthologous variants: 68767939-G-C

7827778-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 68767919-A-T

http://identifiers.org/hco/5/GRCh38#7827851-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68767863-C-A

7827851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: 3 prime UTR variant
orthologous variants: 68767863-C-T

7827877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: 3 prime UTR variant
orthologous variants: 68767837-A-G

7827877-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: 3 prime UTR variant
orthologous variants: 68767837-A-T

7828234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: 3 prime UTR variant
orthologous variants: 68767514-T-C

7828446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: 3 prime UTR variant
orthologous variants: 68767302-A-G

http://identifiers.org/hco/5/GRCh38#7828471-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68767280-C-A

http://identifiers.org/hco/5/GRCh38#7828610-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68767167-C-A

http://identifiers.org/hco/5/GRCh38#7828969-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68766880-C-A

7828969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: 3 prime UTR variant
orthologous variants: 68766880-C-T

7829283-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: 3 prime UTR variant
orthologous variants: 68763158-G-T

http://identifiers.org/hco/5/GRCh38#7829566-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#68762942-C-A

7829566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 233
most severe consequence: 3 prime UTR variant
orthologous variants: 68762942-C-T