7566975-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 8209316-G-C

7566975-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 8209316-G-T

7567188-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 8209506-C-G

7567288-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 8209596-G-C

7567288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 8209596-G-T

7567485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 8209763-G-T

7567621-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 8209878-G-T

7567877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8210098-C-T

7567984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8210193-A-G

7568023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 8210228-C-T

7568028-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 8210230-C-G

http://identifiers.org/hco/7/GRCh38#7568065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8210249-C-A

7568065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 8210249-C-T

http://identifiers.org/hco/7/GRCh38#7568070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8210254-C-A

7568243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8210406-G-T

7568316-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8210483-A-T

7568391-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8210542-G-T

7568431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8210611-G-A

7568539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8210701-A-G

7568592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8210754-C-T

7568601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8210763-A-G

7568685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8210806-G-A

7568722-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8210828-T-A

7568984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8211447-A-G

7569010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8211473-A-G

7569037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8211500-A-G

7569350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8211802-T-C

7569587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8212112-T-C

7569597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8212122-C-T

7569660-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8212184-G-C

7569767-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8212308-G-T

7569965-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8212698-A-T

7570026-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8212763-C-G

7570026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8212763-C-T

http://identifiers.org/hco/7/GRCh38#7570108-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8212939-A-C

7571062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8213585-C-T

7571470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8213930-T-C

7572015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8214373-G-A

7572092-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8214446-G-C

http://identifiers.org/hco/7/GRCh38#7572187-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8214540-C-A

http://identifiers.org/hco/7/GRCh38#7572202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8214555-C-A

http://identifiers.org/hco/7/GRCh38#7572203-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8214556-A-C

7572272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8214628-A-G

7572292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8214649-A-G

7572292-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8214649-A-T

7572295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8214652-G-A

7572295-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8214652-G-T

http://identifiers.org/hco/7/GRCh38#7572433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8214763-C-A

7572433-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 8214763-C-G

7572454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 8214784-C-T

7572601-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 8214931-T-G

7572820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 8215150-A-G

7573222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 8215552-A-G

7573473-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 8215803-C-G

7573473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 8215803-C-T

7573702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 8216032-G-A

7573702-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 8216032-G-C

7573786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8216116-G-A

7573786-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8216116-G-C

7574001-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8216280-A-T

7574015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8216291-T-C

7574057-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8216333-T-C

http://identifiers.org/hco/7/GRCh38#7574208-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8216482-C-A

7574208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8216482-C-T

7574281-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8216549-C-G

7574320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8216597-T-C

http://identifiers.org/hco/7/GRCh38#7574428-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8216700-A-C

7574465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8216736-A-G

http://identifiers.org/hco/7/GRCh38#7574480-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8216753-A-C

7574668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8216923-T-C

7574727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8216968-G-A

7574805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8217048-T-C

7575116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8217125-C-T

7575122-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8217131-G-C

7575368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8217427-A-G

7575608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8217658-T-C

7581475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8220137-C-T

7581583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8220227-G-A

7581704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8220527-C-T

7581797-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 8220614-G-C

7581797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 8220614-G-T

http://identifiers.org/hco/7/GRCh38#7581798-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#8220615-C-A

7581798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 8220615-C-T

7581801-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 8220618-C-G

7581910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8220715-A-G

7581959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8220762-T-C

7582003-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8220807-T-G

7582073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 8220861-A-G

7582074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 8220862-A-G

7582083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 8220871-A-G

7582319-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8221075-C-G

7582426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8221178-T-C

7582605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8221317-T-C

7582642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 8221415-G-A

7582642-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 8221415-G-C

http://identifiers.org/hco/7/GRCh38#7582661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: http://identifiers.org/mco/6/GRCm39#8221434-C-A

7582663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 8221436-G-A

7582663-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 8221436-G-T

7582664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 8221437-G-A

7582664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 8221437-G-T

7582681-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 8221456-A-T

7582696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 8221471-A-G

http://identifiers.org/hco/7/GRCh38#7582727-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8221498-A-C

7582727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 8221498-A-G

7582727-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 8221498-A-T

7582731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 8221502-G-A

7582731-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 8221502-G-T

http://identifiers.org/hco/7/GRCh38#7582782-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8221530-A-C

7582782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 8221530-A-G

7582782-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 8221530-A-T

http://identifiers.org/hco/7/GRCh38#7582874-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8221606-C-A

7582938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8222291-C-T

7583004-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8222343-T-A

http://identifiers.org/hco/7/GRCh38#7583011-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8222350-C-A

7583011-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8222350-C-G

7583011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8222350-C-T

7583065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8222401-C-T

7583152-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 8222495-G-T

7583203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 8222546-T-C

7583235-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 8222578-C-G

7583235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 8222578-C-T

7583272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 8222615-A-G

7583415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8222740-T-C

7583417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8222742-A-G

7583461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8222786-A-G

7583521-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8222831-T-G

http://identifiers.org/hco/7/GRCh38#7583524-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8222835-C-A

7583524-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8222835-C-G

7583527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8222838-T-C

7583586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8222900-G-A

7583586-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8222900-G-T

http://identifiers.org/hco/7/GRCh38#7583659-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8222974-A-C

7583659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8222974-A-G

7583721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8223023-T-C

7584237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8223525-C-T

7584301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8223586-A-G

7584916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8223857-T-C

7585109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8224041-T-C

http://identifiers.org/hco/7/GRCh38#7585153-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8224081-A-C

7585262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8224170-A-G

7585568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8224488-T-C

7585588-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8224509-T-G

http://identifiers.org/hco/7/GRCh38#7585595-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8224516-C-A

7585596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8224517-T-C

7585697-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 8224616-C-G

7585766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 8224685-A-G

7585824-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8224743-T-G

7585842-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8224761-T-A

http://identifiers.org/hco/7/GRCh38#7585944-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8224769-C-A

7585944-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8224769-C-G

7585944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8224769-C-T

7586131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8224883-C-T

7586172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8224910-G-A

7586277-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8224989-C-G

http://identifiers.org/hco/7/GRCh38#7586561-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8225257-A-C

http://identifiers.org/hco/7/GRCh38#7586794-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8225476-C-A

7586813-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8225495-A-T

7586972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8225627-A-G

http://identifiers.org/hco/7/GRCh38#7587535-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8225805-C-A

7587616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8225887-A-G

7587795-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8226035-A-T

7587824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8226064-C-T

7588035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8226317-G-T

7588040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8226322-G-A

7588040-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8226322-G-T

7588363-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8226763-T-A

7588363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8226763-T-C

http://identifiers.org/hco/7/GRCh38#7588490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8226836-C-A

7588490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 8226836-C-T

http://identifiers.org/hco/7/GRCh38#7588644-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8226994-C-A

7588644-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8226994-C-G

7588644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8226994-C-T

7588724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8227061-A-G

7588916-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8227223-T-G

7588992-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8227282-G-C

7588994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8227284-G-A

7589071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8227347-A-G

7589536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 8228100-T-C

http://identifiers.org/hco/7/GRCh38#7589620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8228175-C-A

7589620-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8228175-C-G

7589620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8228175-C-T

7589659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8228214-A-G

7589659-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8228214-A-T

7589676-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8228219-A-T

7589932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8228479-A-G

7589976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8228524-A-G

7589982-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8228530-G-T

7589983-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8228531-G-T

7590285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8228806-C-T

7590385-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8228898-G-T

7590624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8229099-T-C

7590722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8229234-A-G

7590847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8229328-T-C

7590914-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8229402-G-C

7590952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8229438-C-T

7591164-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8229687-C-G

http://identifiers.org/hco/7/GRCh38#7591226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8229739-C-A

7591258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8229769-T-C

7591283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8229794-T-C

7591283-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8229794-T-G

7591295-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8229806-G-C

7591297-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8229808-G-T

7594673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8230901-A-G

7594824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8231056-A-G

7594825-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8231057-T-A

7594825-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8231057-T-G

7594834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8231065-T-C

http://identifiers.org/hco/7/GRCh38#7594837-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8231070-A-C

7594837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8231070-A-G

7594837-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8231070-A-T

http://identifiers.org/hco/7/GRCh38#7594851-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8231084-C-A

7594851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8231084-C-T

http://identifiers.org/hco/7/GRCh38#7594852-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8231085-C-A

7594852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8231085-C-T

http://identifiers.org/hco/7/GRCh38#7594912-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8231092-C-A

7594912-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8231092-C-G

7594912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8231092-C-T

http://identifiers.org/hco/7/GRCh38#7594926-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8231106-C-A

7594928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8231108-G-A

http://identifiers.org/hco/7/GRCh38#7594950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8231131-C-A

7594950-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8231131-C-G

7594963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8231144-T-C

7594963-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8231144-T-G

http://identifiers.org/hco/7/GRCh38#7595168-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8231349-C-A

7595177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8231357-G-A

7595177-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8231357-G-T

http://identifiers.org/hco/7/GRCh38#7595214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8231387-C-A

7595214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8231387-C-T

7595270-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8231436-A-T

7595277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8231443-T-C

7595352-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8231521-C-G

http://identifiers.org/hco/7/GRCh38#7595421-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8231625-C-A

7595421-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8231625-C-G

7595431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8231635-A-G

7595455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8231643-G-A

7595465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8231653-G-A

7595475-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8231663-G-C

http://identifiers.org/hco/7/GRCh38#7595522-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8231703-C-A

7595987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8232802-A-G

7596091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8232914-G-A

http://identifiers.org/hco/7/GRCh38#7596116-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8232939-C-A

7596152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8232969-G-A

7596152-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8232969-G-T

7596170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8232974-A-G

7596180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8232984-G-A

7596180-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8232984-G-T

http://identifiers.org/hco/7/GRCh38#7596190-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8232994-C-A

7596190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8232994-C-T

http://identifiers.org/hco/7/GRCh38#7596209-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8233006-C-A

7596209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8233006-C-T

7596412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 8233205-A-G

7596412-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 8233205-A-T

7596421-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 8233214-T-G

http://identifiers.org/hco/7/GRCh38#7596480-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8233271-A-C

7596480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8233271-A-G

7596606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8233370-A-G

7596892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8233621-C-T

7597447-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8233684-T-A

7597447-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8233684-T-G

7605802-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8234100-C-G

7605857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8234154-A-G

7605857-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8234154-A-T

http://identifiers.org/hco/7/GRCh38#7605874-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8234171-C-A

7605874-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8234171-C-G

7605874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8234171-C-T

7605887-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8234182-A-T

7605905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8234195-T-C

7605905-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8234195-T-G

7605918-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8234208-G-T

7606027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 8234317-T-C

7606080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8234370-C-T

7606103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8234394-G-A

7606103-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8234394-G-C

7606152-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8234446-T-A

7606152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8234446-T-C

7606390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8234782-C-T

7606424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8234813-A-G

7606424-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8234813-A-T

7606557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8234929-A-G

7606695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8235239-A-G

7606977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8235369-A-G

7607195-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 8235572-G-T

http://identifiers.org/hco/7/GRCh38#7607198-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8235575-A-C

7607198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 8235575-A-G

7607202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 8235579-G-A

7607202-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 8235579-G-C

7607202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 8235579-G-T

7607238-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 8235614-G-T

7607273-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 8235649-T-A

7607274-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 8235650-G-T

http://identifiers.org/hco/7/GRCh38#7607375-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8235743-C-A

7607375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 8235743-C-T

7607569-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 8235919-T-A

7607569-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 8235919-T-G

http://identifiers.org/hco/7/GRCh38#7607693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8235993-C-A

7607759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 8236063-C-T

7607921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 8236411-T-C

7607930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 8236420-A-G

http://identifiers.org/hco/7/GRCh38#7607972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8236460-C-A

http://identifiers.org/hco/7/GRCh38#7608090-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8236552-C-A

7608124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 8236587-G-A

http://identifiers.org/hco/7/GRCh38#7608146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8236608-C-A

7608175-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 8236634-C-G

7608175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 8236634-C-T

7608242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 8236684-C-T

7608289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 8236726-T-C

http://identifiers.org/hco/7/GRCh38#7608505-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8236892-A-C

7608611-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 8236989-G-C

7608611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 8236989-G-T

7608623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 8237034-A-G

7608626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 8237037-G-T

http://identifiers.org/hco/7/GRCh38#7608627-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8237038-A-C

7608798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 8237308-T-C

7609081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21905
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 8237619-A-G