http://identifiers.org/hco/12/GRCh38#30926432-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#127864571-A-C

30926432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 127864571-A-G

30926432-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 127864571-A-T

30926708-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 5 prime UTR variant
orthologous variants: 127864761-G-C

30926711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 5 prime UTR variant
orthologous variants: 127864764-G-A

30926711-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 5 prime UTR variant
orthologous variants: 127864764-G-T

http://identifiers.org/hco/12/GRCh38#30926832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#127864875-C-A

30926832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 127864875-C-T

30926850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127864904-G-A

30926850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127864904-G-T

http://identifiers.org/hco/12/GRCh38#30926867-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127864921-C-A

30926867-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127864921-C-G

30926867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127864921-C-T

30926882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 127864936-G-A

30926882-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 127864936-G-T

30926929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 127864957-G-A

30926929-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 127864957-G-C

30926929-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 127864957-G-T

30926951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127864992-G-A

30926951-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127864992-G-T

30927073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127865090-A-G

30927073-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127865090-A-T

30927135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127865153-G-A

30927135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127865153-G-T

30927207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127865266-C-T

30927214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127865303-G-A

30927431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 127865504-T-C

30927574-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127865620-T-G

30927579-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127865625-T-G

30927598-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127865642-T-G

30927968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127865995-G-A

30927979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127866007-C-T

30928005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127866031-C-T

30928023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127866049-A-G

30928390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127866388-G-A

30930062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127866797-A-G

30930188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127866913-T-C

30930247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127866977-C-T

http://identifiers.org/hco/12/GRCh38#30930691-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127867299-A-C

30930695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127867303-G-A

30930695-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127867303-G-T

30930704-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127867312-C-G

30930712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127867322-G-A

30931062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127867945-G-A

30931087-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127867966-T-C

30931106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127867987-C-T

30931121-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127868002-C-G

30931121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127868002-C-T

30931154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127868010-T-C

30931353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127868239-G-T

30931379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127868255-G-A

30931994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127868522-T-C

http://identifiers.org/hco/12/GRCh38#30932099-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127868631-A-C

30932616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127871442-G-A

30932832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127871677-A-G

30932966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127871806-A-G

30932997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127871836-A-G

30935017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127873136-C-T

30935108-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127873209-T-A

30935308-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127873389-T-G

30936225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127873927-C-T

30936555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127874226-G-A

30936586-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127874256-T-G

30936701-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127874342-T-G

http://identifiers.org/hco/12/GRCh38#30936776-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127874398-C-A

30936795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127874417-T-C

30937080-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127875400-G-T

30940570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127876818-T-C

30940589-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127876850-G-C

30941770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127877477-A-G

30941962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127877609-T-C

30942335-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127878801-G-C

30942509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127878964-G-A

30942911-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127879731-C-G

30942955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127879779-C-T

30943165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127879956-C-T

30945670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127881039-A-G

30945752-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127881136-G-C

30945752-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127881136-G-T

30945834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127881205-T-C

30945871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127881222-C-T

30945920-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127881269-G-C

30945920-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127881269-G-T

30946559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127881841-T-C

30946605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127881915-G-A

30946625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127881935-G-A

30946631-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127881941-G-T

30952776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127889928-T-C

30952777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127889929-C-T

30953237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127889238-A-G

30953240-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127889241-G-C

30953240-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127889241-G-T

30953337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127889333-C-T

30953477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127889451-C-T

30953633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127889632-G-A

http://identifiers.org/hco/12/GRCh38#30953660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127889653-C-A

30953805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127889751-G-T

30953809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127889755-T-C

http://identifiers.org/hco/12/GRCh38#30953843-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127889782-C-A

30953843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127889782-C-T

30953850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127889795-A-G

http://identifiers.org/hco/12/GRCh38#30953862-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127889805-C-A

30953862-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127889805-C-G

30953862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127889805-C-T

30953882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127889809-G-A

30953882-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127889809-G-C

30953882-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127889809-G-T

30953924-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127889855-G-T

30953996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 127889928-C-T

30954167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127890087-A-G

30955198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127891685-T-C

30956472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127893954-T-C

30956472-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127893954-T-G

30956770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127894182-T-C

30956828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127894240-C-T

30956832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127894244-C-T

30956850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127894262-A-G

30956878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127894302-C-T

30959057-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127895494-C-G

30959207-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127895569-T-G

30959210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127895572-G-A

30959547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127895905-A-G

30959613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127895971-G-A

30959675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127896031-G-A

30959687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127896043-G-A

30959727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127896095-C-T

http://identifiers.org/hco/12/GRCh38#30959760-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127896142-A-C

30959760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127896142-A-G

30959765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127896149-G-A

30959765-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127896149-G-T

http://identifiers.org/hco/12/GRCh38#30959771-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127896155-C-A

http://identifiers.org/hco/12/GRCh38#30959815-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127896283-A-C

30959815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127896283-A-G

30959957-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127896433-A-T

30960008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127896479-G-A

30960009-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127896480-G-T

30960061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127896531-G-A

30960135-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127896593-T-A

30960135-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127896593-T-G

30960150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127896599-G-A

30960155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127896604-G-A

30960155-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127896604-G-C

30960199-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127896646-T-C

30960390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127896814-G-A

30960578-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127896996-G-C

30961707-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127898532-G-C

30961828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127898653-C-T

30961960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127898819-G-A

30961995-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127898853-T-A

30962023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127898875-A-G

30962057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127898912-A-G

30962225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127899081-T-C

30962239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127899094-C-T

30962541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127899376-A-G

30962627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127899501-G-A

30962760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127899643-T-C

30962784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127899666-G-A

30962871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127899744-C-T

30962985-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127899838-C-G

30963207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127900015-C-T

30963425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127900170-G-T

30963698-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127900392-T-A

http://identifiers.org/hco/12/GRCh38#30963704-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127900398-C-A

30963704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127900398-C-T

30963726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127900418-G-A

30963726-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127900418-G-T

30963731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127900423-T-C

30963752-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127900444-C-G

30963752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127900444-C-T

30963794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127900486-A-G

30963794-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127900486-A-T

http://identifiers.org/hco/12/GRCh38#30963840-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127900529-C-A

30963840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 127900529-C-T

30964033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127900720-G-A

30964112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127900805-A-G

30964112-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127900805-A-T

30964126-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127900849-T-A

30964126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127900849-T-C

30964156-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127900877-T-A

30964156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127900877-T-C

30964163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127900884-G-A

30964163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127900884-G-T

30964209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127900931-G-A

30964294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127901032-T-C

30964296-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127901034-C-G

30964314-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127901052-T-G

http://identifiers.org/hco/12/GRCh38#30964319-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127901057-C-A

http://identifiers.org/hco/12/GRCh38#30964370-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127901109-A-C

http://identifiers.org/hco/12/GRCh38#30965076-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127902586-A-C

30965121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127902625-G-A

30965174-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127902672-T-A

30965229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127902725-G-A

30965319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127902788-C-T

30965320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127902789-T-C

30965324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127902793-G-A

30965536-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127903023-T-A

30965601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127903092-G-T

30965635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127903127-A-G

30966775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127907253-C-T

30967040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127907016-A-G

http://identifiers.org/hco/12/GRCh38#30967291-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127906750-C-A

30967447-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127906607-G-C

http://identifiers.org/hco/12/GRCh38#30967813-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127906310-C-A

30967813-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127906310-C-G

30967813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127906310-C-T

30967909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127906215-G-A

30968230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127905919-A-G

30968306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127905835-G-A

30968412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127905729-G-A

30968412-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127905729-G-T

30968490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127905656-C-T

30968568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127905383-G-A

30968988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127904917-T-C

30969024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127904881-G-A

30969163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127904772-G-A

30969163-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127904772-G-C

30969344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127904611-C-T

30969976-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127908948-G-T

30970055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127909086-A-G

30970227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127909265-G-A

30970227-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127909265-G-C

30970236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127909274-G-A

30970260-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127909295-C-G

30970260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127909295-C-T

30970737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127909706-C-T

30970778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127909747-C-T

30971078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127910031-G-A

30971082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127910035-G-A

30971131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127910081-G-A

30971192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127910148-C-T

30971799-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127910446-T-A

30971872-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127910519-G-C

30971882-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127910529-C-G

30971882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127910529-C-T

30974582-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127911608-G-C

30974605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127911629-G-A

30974623-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127911646-T-C

30974643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127911658-C-T

30975164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127912085-G-A

30975459-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127912417-C-G

30975459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127912417-C-T

30975565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127912511-A-G

http://identifiers.org/hco/12/GRCh38#30975599-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127912535-A-C

30975841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127912745-G-A

30975955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127912879-T-C

30975986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127912910-G-A

30976132-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127913009-T-A

http://identifiers.org/hco/12/GRCh38#30976148-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127913021-A-C

30976274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127913147-G-A

30976280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127913172-T-C

30976598-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127913502-T-G

30976697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127913575-C-T

30976919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127913785-G-A

http://identifiers.org/hco/12/GRCh38#30976977-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127913843-C-A

http://identifiers.org/hco/12/GRCh38#30977004-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127913868-C-A

30977115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127913987-G-A

30977254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127914074-C-T

30977882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 127914546-G-A

30977923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127914586-G-A

30977953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127914617-G-A

30978016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 127914656-A-G

http://identifiers.org/hco/12/GRCh38#30978161-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#127914764-C-A

30978161-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 127914764-C-G

30978214-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 127914803-G-T

30978215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 127914804-T-C

http://identifiers.org/hco/12/GRCh38#30978298-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127914878-C-A

30978311-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127914891-G-C

http://identifiers.org/hco/12/GRCh38#30978320-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127914900-C-A

30978320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127914900-C-T

30978330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127914910-A-G

30978425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127915011-G-T

30978435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127915041-G-T

30978490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127915094-C-T

http://identifiers.org/hco/12/GRCh38#30978523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127915127-C-A

30978523-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127915127-C-G

30978523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127915127-C-T

30978658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127915261-G-A

30978658-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127915261-G-C

http://identifiers.org/hco/12/GRCh38#30978682-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127915285-A-C

30978694-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127915294-T-G

http://identifiers.org/hco/12/GRCh38#30978786-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127915381-C-A

30978786-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127915381-C-G

30978786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127915381-C-T

30978817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127915411-G-T

30978833-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127915427-T-A

http://identifiers.org/hco/12/GRCh38#30978842-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127915436-C-A

30978851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127915445-G-T

http://identifiers.org/hco/12/GRCh38#30978930-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127915526-A-C

30978930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127915526-A-G

30978933-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127915529-T-A

30979052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127915636-T-C

http://identifiers.org/hco/12/GRCh38#30979060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127915644-C-A

30979060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127915644-C-T

http://identifiers.org/hco/12/GRCh38#30979061-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127915645-A-C

30979065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127915649-T-C

30979248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127915847-T-C

30979248-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127915847-T-G

30979287-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127915873-T-A

30979294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127915886-C-T

http://identifiers.org/hco/12/GRCh38#30979298-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127915890-A-C

30979484-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127915989-G-T

30979530-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127916026-T-A

30979752-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127916230-T-A

30979752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127916230-T-C

30980743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127916647-C-T

30980744-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127916648-C-G

30980744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127916648-C-T

30981123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127916942-G-A

30981167-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127916983-G-C

30981202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127917018-G-A

30981603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127919464-G-A

30981603-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127919464-G-T

30981764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127919577-T-C

30981917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127919706-A-G

30982070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127919800-A-G

30982442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127920080-G-T

30982446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127920084-G-A

30982446-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127920084-G-C

http://identifiers.org/hco/12/GRCh38#30982503-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127920157-C-A

30982503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127920157-C-T

http://identifiers.org/hco/12/GRCh38#30982576-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127920224-C-A

30982579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 127920227-G-A

30982703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127920351-G-A

30982721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127920366-G-A

30982721-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127920366-G-T

http://identifiers.org/hco/12/GRCh38#30982924-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127920529-C-A

30982924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127920529-C-T

30982951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127920553-G-A

30982951-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127920553-G-T

30982966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127920565-G-A

30982966-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127920565-G-C

30982966-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127920565-G-T

http://identifiers.org/hco/12/GRCh38#30983003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127920608-C-A

30983003-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127920608-C-G

30983003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127920608-C-T

30983035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127920640-T-C

http://identifiers.org/hco/12/GRCh38#30983255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127920826-C-A

30983255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127920826-C-T

http://identifiers.org/hco/12/GRCh38#30983271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127920840-C-A

30983271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127920840-C-T

http://identifiers.org/hco/12/GRCh38#30983292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127920849-C-A

30983292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127920849-C-T

30983539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127921050-A-G

30983551-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127921057-G-T

30983564-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127921070-A-T

http://identifiers.org/hco/12/GRCh38#30985127-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127921944-A-C

30985246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127922065-G-A

30985313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127922110-A-G

30985738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127922470-T-C

30985751-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127922486-C-G

http://identifiers.org/hco/12/GRCh38#30985935-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127922855-A-C

30985935-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127922855-A-T

30985987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127922913-G-A

30986052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127922977-G-A

30986100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127923031-G-T

30986111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127923042-C-T

30986343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127923255-T-C

30986544-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127923438-A-T

30988747-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127923994-A-T

30988766-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127924013-G-C

30988814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127924068-C-T

30988908-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127924151-T-G

30989041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127924284-C-T

30989131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127924360-G-A

30989131-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127924360-G-C

30989148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127924374-G-A

30989402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127924621-G-A

30989424-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127924645-C-G

30989458-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127924668-G-T

30989663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127924794-T-C

30989684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127924815-G-A

30989866-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 127924983-A-T

http://identifiers.org/hco/12/GRCh38#30990126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#127925243-C-A

30990126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 127925243-C-T

30990137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 127925265-C-T

30990138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 127925266-G-A

30990146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 127925274-G-A

30990149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127925277-T-C

30990157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127925285-T-C

30991318-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127926234-A-T

30991411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127926321-A-G

30991573-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127926500-G-C

30991626-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127926551-G-C

30991652-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127926581-G-C

30991656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127926587-C-T

30991719-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127926636-G-T

http://identifiers.org/hco/12/GRCh38#30991753-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127926669-C-A

30991753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127926669-C-T

30991759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127926675-G-A

30991797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127926701-G-A

30991797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127926701-G-T

30991828-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127926730-T-G

http://identifiers.org/hco/12/GRCh38#30992088-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127926971-A-C

30992088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127926971-A-G

30992088-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127926971-A-T

http://identifiers.org/hco/12/GRCh38#30992108-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127926988-C-A

30992108-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127926988-C-G

30992108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127926988-C-T

30992180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127927064-C-T

30992191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127927075-G-T

http://identifiers.org/hco/12/GRCh38#30992213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127927096-C-A

30992213-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127927096-C-G

30992213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127927096-C-T

30992219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127927102-G-A

30992219-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127927102-G-T

30992238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127927123-G-A

30992238-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127927123-G-T

30992241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127927126-C-T

30992249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127927134-G-A

http://identifiers.org/hco/12/GRCh38#30992267-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127927156-A-C

30992267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127927156-A-G

http://identifiers.org/hco/12/GRCh38#30992272-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127927161-C-A

30992394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127927282-C-T

http://identifiers.org/hco/12/GRCh38#30992418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127927298-C-A

30992418-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127927298-C-G

30992463-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127927323-T-A

30992463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127927323-T-C

30992464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127927324-G-A

30992464-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127927324-G-T

30992471-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127927330-T-G

30992472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127927331-T-C

http://identifiers.org/hco/12/GRCh38#30992486-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127927345-C-A

30992486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127927345-C-T

30992489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127927348-A-G

http://identifiers.org/hco/12/GRCh38#30992536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127927398-C-A

30992536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127927398-C-T

30992545-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127927407-G-T

30992622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127927439-G-A

30992626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127927443-G-A

http://identifiers.org/hco/12/GRCh38#30992696-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127927484-C-A

30992759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127927529-G-T

30992769-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127927540-T-A

30992769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127927540-T-C

30992777-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127927552-T-A

30992777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127927552-T-C

http://identifiers.org/hco/12/GRCh38#30992797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127927564-C-A

30992823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127927590-A-G

30992828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127927601-T-C

30992924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127927679-C-T

30992956-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127927710-G-T

30993047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127927785-C-T

30993167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127927895-A-G

30993172-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127927900-T-G

http://identifiers.org/hco/12/GRCh38#30993188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127927920-C-A

30993188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127927920-C-T

30993209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127927941-G-A

30993209-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127927941-G-C

30993209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127927941-G-T

30993277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127927991-C-T

30993288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127928001-T-C

http://identifiers.org/hco/12/GRCh38#30993289-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127928002-C-A

30993331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127928048-C-T

30993414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127928129-G-T

30993485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127928190-G-A

30993487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127928192-G-A

30993513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127928217-G-A

30993592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127928277-T-C

30993626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127928324-A-G

http://identifiers.org/hco/12/GRCh38#30993666-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127928347-C-A

30993666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127928347-C-T

30993797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127928434-G-T

30993904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127928553-A-G

30994037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127928612-C-T

30994038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127928613-G-A

30994038-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127928613-G-T

30994081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127928627-A-G

30994164-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127928701-G-T

30994215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127928743-G-A

30994278-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127928783-A-T

30994303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127928824-G-A

30994303-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127928824-G-C

30994309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127928830-C-T

30994327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127928845-A-G

30994441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127928956-A-G

http://identifiers.org/hco/12/GRCh38#30994485-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127928993-A-C

30994502-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127929010-G-T

http://identifiers.org/hco/12/GRCh38#30994518-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127929025-A-C

30994518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127929025-A-G

30994518-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127929025-A-T

30994519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127929026-C-T

http://identifiers.org/hco/12/GRCh38#30994533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127929040-C-A

30994533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127929040-C-T

30994550-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127929056-G-T

http://identifiers.org/hco/12/GRCh38#30994624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127929124-C-A

http://identifiers.org/hco/12/GRCh38#30994758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127929196-C-A

30994768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127929201-T-C

30994861-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127929287-G-T

http://identifiers.org/hco/12/GRCh38#30994913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127929337-C-A

30994913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127929337-C-T

http://identifiers.org/hco/12/GRCh38#30994914-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127929338-C-A

30994914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127929338-C-T

http://identifiers.org/hco/12/GRCh38#30994937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127929352-C-A

30994937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127929352-C-T

30995000-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127929408-G-T

30995005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127929413-A-G

http://identifiers.org/hco/12/GRCh38#30995029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127929437-C-A

30995029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127929437-C-T

30995065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127929516-A-G

30995070-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127929521-G-T

30995147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127929575-A-G

30995192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127929619-G-A

30995205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127929632-G-A

30995205-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127929632-G-T

http://identifiers.org/hco/12/GRCh38#30995257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127929675-C-A

30995257-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127929675-C-G

30995257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127929675-C-T

30995405-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127929809-G-T

30995410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127929814-C-T

30995430-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127929837-G-T

30995487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127929880-C-T

30995612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127929985-G-T

30995647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127929993-G-A

30995684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127930028-T-C

http://identifiers.org/hco/12/GRCh38#30995821-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127930210-C-A

30995821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127930210-C-T

30995973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127930357-G-A

30995973-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127930357-G-T

30996011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127930396-C-T

http://identifiers.org/hco/12/GRCh38#30996012-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127930397-C-A

30996012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127930397-C-T

30996046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127930433-T-C

http://identifiers.org/hco/12/GRCh38#30996089-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127930472-C-A

30996089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127930472-C-T

http://identifiers.org/hco/12/GRCh38#30996364-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127930720-C-A

30996364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127930720-C-T

30996376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127930732-C-T

30996382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127930738-G-A

30996393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127930748-T-C

http://identifiers.org/hco/12/GRCh38#30996399-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127930754-C-A

30996399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127930754-C-T

30996407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127930762-A-G

http://identifiers.org/hco/12/GRCh38#30996410-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127930765-C-A

http://identifiers.org/hco/12/GRCh38#30996503-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#127930857-A-C

30996503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127930857-A-G

30996521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 127930873-T-C

30996643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127930978-G-A

30996891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127931194-T-C

30998599-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127933316-G-C

30998701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127933411-G-T

31001672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30795
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127937092-G-A