134127303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 34006326-G-A

134127303-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 34006326-G-T

134127323-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 34006346-T-A

134127323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 34006346-T-C

http://identifiers.org/hco/7/GRCh38#134127327-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#34006350-C-A

134127327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 34006350-C-T

http://identifiers.org/hco/7/GRCh38#134127383-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#34006407-A-C

134127383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 34006407-A-G

134127406-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 34006430-T-A

134127406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 34006430-T-C

134127406-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 34006430-T-G

http://identifiers.org/hco/7/GRCh38#134127415-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#34006439-C-A

134127415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 34006439-C-T

134127420-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 34006444-G-C

http://identifiers.org/hco/7/GRCh38#134127479-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#34006503-C-A

134127479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 34006503-C-T

134127503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 34006530-A-G

134127568-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 34006595-C-G

http://identifiers.org/hco/7/GRCh38#134127685-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#34006713-C-A

134127685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34006713-C-T

134127721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34006759-C-T

http://identifiers.org/hco/7/GRCh38#134127742-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#34006778-C-A

134127742-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34006778-C-G

134127742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34006778-C-T

134127949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34006973-T-C

134127950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34006974-A-G

134128112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34007063-A-G

134128184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34007127-A-G

134128296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34007251-T-C

134128475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34007367-C-T

134130379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34008226-C-T

134130615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34008430-A-G

134130635-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34008450-C-G

134130636-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34008451-C-G

134130638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34008453-A-G

134130741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34008514-A-G

134131077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34009031-G-A

134131077-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34009031-G-T

134131126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34009074-G-T

134131142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34009090-C-T

134131143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34009091-A-G

134131371-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34009328-T-A

134131379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34009330-C-T

134131423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34009371-G-A

134131955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34009898-G-A

134135027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34010559-G-A

134135037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34010570-A-G

http://identifiers.org/hco/7/GRCh38#134136091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#34012204-C-A

http://identifiers.org/hco/7/GRCh38#134136210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#34012316-C-A

134136214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34012320-C-T

134136221-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34012327-C-G

134136221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34012327-C-T

134136223-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34012329-C-G

http://identifiers.org/hco/7/GRCh38#134136424-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#34012481-A-C

134136424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34012481-A-G

134136425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34012482-T-C

134136483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34012540-T-C

134136592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34012627-C-T

134136783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34012774-A-G

http://identifiers.org/hco/7/GRCh38#134136958-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#34013378-C-A

http://identifiers.org/hco/7/GRCh38#134136973-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#34013393-C-A

134137055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 34013468-T-C

134137063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 34013476-A-G

134137178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34013582-T-C

134137224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34013621-G-A

134137224-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34013621-G-T

http://identifiers.org/hco/7/GRCh38#134137238-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#34013635-C-A

134137250-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34013647-G-T

134137598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34013980-A-G

134137669-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34014053-A-G

134138027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34014646-T-C

134138093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34014710-A-G

134138095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34014712-A-G

134138280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34014897-G-A

134138454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34015079-C-T

134138515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34015139-A-G

134138720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34015350-C-T

134138835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34015465-T-C

134139016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34015535-T-C

134139035-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34015554-G-C

134139073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34015591-A-G

http://identifiers.org/hco/7/GRCh38#134139295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#34015923-C-A

134139295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34015923-C-T

134139329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34016127-A-G

134139346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34016144-T-C

134139346-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34016144-T-G

134139360-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34016158-T-A

134139360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34016158-T-C

134140224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34016757-C-T

134140255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34016763-C-T

134140256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34016764-C-T

134140348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34016859-A-G

134140562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34017055-A-G

134140578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34017071-C-T

134140708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34017200-A-G

http://identifiers.org/hco/7/GRCh38#134140840-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#34017326-A-C

134141048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34017567-G-A

134141051-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34017570-G-C

134141052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34017571-G-A

134141218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34017745-T-C

134141222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34017749-T-C

134141273-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34017810-T-G

134141334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34017881-T-C

134141354-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34017902-G-T

134141501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34018034-C-T

134141571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34018114-T-C

http://identifiers.org/hco/7/GRCh38#134141591-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#34018134-C-A

134141591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34018134-C-T

http://identifiers.org/hco/7/GRCh38#134141601-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#34018144-C-A

134141601-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34018144-C-G

134141601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34018144-C-T

134141757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34018297-G-A

134141806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34018371-C-T

134141847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34018415-A-G

134141853-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34018421-T-G

134142278-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34019120-C-G

134142368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34019190-G-A

http://identifiers.org/hco/7/GRCh38#134142491-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#34019306-A-C

134142766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34019588-C-T

134142859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34019684-T-C

134142927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34020070-C-T

http://identifiers.org/hco/7/GRCh38#134142929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#34020072-C-A

134142929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34020072-C-T

134142967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34020110-T-C

134143047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34020325-T-C

134143048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34020326-G-A

134143048-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34020326-G-C

134143120-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 34020398-T-A

134143224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34020497-A-G

134143250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34020514-G-A

134143250-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34020514-G-C

134143266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34020531-G-A

134143271-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34020536-A-T

134143302-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34020567-A-T

134143406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34020658-T-C

134143416-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34020668-T-A

http://identifiers.org/hco/7/GRCh38#134144669-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#34023153-A-C

134144829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34023574-G-A

134144829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34023574-G-T

134145141-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34023855-G-C

134145560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34023949-A-G

134145632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34024029-T-C

134145787-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34024171-G-C

134145830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34024220-C-T

134145930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34024372-C-T

http://identifiers.org/hco/7/GRCh38#134146369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#34024507-C-A

134146447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34024557-A-G

134146656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34024779-G-A

134146671-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34024798-T-G

134146823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34024895-G-A

134146982-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34025046-A-T

http://identifiers.org/hco/7/GRCh38#134147413-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#34025198-C-A

134147413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34025198-C-T

134147578-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34025308-T-C

134147970-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34025513-G-T

134147979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34025522-T-C

134148080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34025633-A-G

134148080-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34025633-A-T

134148141-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34025700-T-A

134148154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34025713-A-G

134148217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34025774-T-C

134148446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34025987-A-G

134148446-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34025987-A-T

134149364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34026626-G-A

134149579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34026816-A-G

134149674-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34026893-T-G

134149718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34026964-G-A

134153222-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34029474-T-A

134153222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34029474-T-C

134153556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34029778-C-T

134154339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34030581-G-A

134154548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34030995-G-T

134154672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34031110-T-C

134154738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34031170-G-A

134154738-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34031170-G-C

134155028-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34031335-G-C

134155033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34031340-G-A

134155687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34031964-G-A

134155687-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34031964-G-C

134155687-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34031964-G-T

134157386-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34032480-C-G

134157386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34032480-C-T

134157423-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34032518-C-G

http://identifiers.org/hco/7/GRCh38#134157428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#34032523-C-A

134157428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34032523-C-T

134157822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34032606-C-T

http://identifiers.org/hco/7/GRCh38#134157898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#34032673-C-A

134158074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 34033045-A-G

134158176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34033147-G-A

134158176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34033147-G-T

134158179-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34033150-G-C

134158185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34033156-T-C

134158228-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34033197-G-T

http://identifiers.org/hco/7/GRCh38#134158230-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#34033199-C-A

134158288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34033258-G-A

http://identifiers.org/hco/7/GRCh38#134158305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#34033275-C-A

134158951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34033905-G-A

http://identifiers.org/hco/7/GRCh38#134158961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#34033915-C-A

134158961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34033915-C-T

134159420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34034270-A-G

134159833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34034337-T-C

134160036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34034538-T-C

134160698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34035338-G-A

134160700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34035340-A-G

134161042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34035692-A-G

134161318-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34035892-T-A

134161667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34036227-G-A

134161689-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34036302-T-A

134161689-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34036302-T-G

134162039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34036773-A-G

134162074-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34036810-T-A

134163303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34039191-A-G

134163327-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34039215-T-A

134163327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34039215-T-C

134163364-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34039252-T-A

http://identifiers.org/hco/7/GRCh38#134163551-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#34039463-A-C

134163551-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34039463-A-T

134163573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34039495-T-C

134163592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34039515-A-G

http://identifiers.org/hco/7/GRCh38#134163613-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#34039536-C-A

http://identifiers.org/hco/7/GRCh38#134163642-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#34039761-C-A

134163643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34039762-A-G

134163649-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34039768-T-A

134163649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34039768-T-C

134163650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34039769-G-A

http://identifiers.org/hco/7/GRCh38#134163655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#34039774-C-A

134163665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34039784-T-C

134163925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34040034-C-T

134164035-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34040153-A-T

134164312-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34040559-A-T

134164341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34040590-C-T

134164968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34041195-T-C

134165109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34041337-A-G

134165577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34041849-A-G

134165667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34041953-T-C

134166014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34042203-C-T

134166046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34042233-C-T

134166156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34042342-C-T

134166229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34042419-G-A

134166229-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34042419-G-T

134166738-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34042952-C-G

134166813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34043016-A-G

134166948-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34043139-A-T

134167002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34043259-T-C

134167197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34043409-C-T

134167622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34043775-G-A

134167962-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34043971-C-G

134167997-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34044004-A-T

134168060-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34044077-G-T

134168643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34044523-T-C

134168727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34044603-G-A

134168727-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34044603-G-T

134169032-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34044869-G-T

134169073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34044905-A-G

134169266-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34045178-G-C

134169448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34045351-C-T

134169736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34045652-T-C

134169841-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34045777-T-G

134170044-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34045973-C-G

134170065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34045994-T-C

http://identifiers.org/hco/7/GRCh38#134170084-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#34046015-A-C

134170142-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34046145-G-C

134170172-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34046256-C-G

134170214-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34046300-T-A

134170214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34046300-T-C

134170338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34046421-T-C

134173261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34047075-A-G

134174077-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34047653-C-G

http://identifiers.org/hco/7/GRCh38#134174078-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#34047654-C-A

134174212-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34047746-T-G

134174644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 34048084-A-G

134174662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34048104-G-A

http://identifiers.org/hco/7/GRCh38#134174714-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#34048146-A-C

134174935-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34048354-G-C

134176843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34049174-A-G

134176860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34049191-T-C

134176860-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34049191-T-G

134176870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34049198-T-C

134177074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34049402-A-G

134177125-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34049446-G-T

http://identifiers.org/hco/7/GRCh38#134177172-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#34049491-A-C

134177172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34049491-A-G

134177172-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34049491-A-T

134177176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34049495-G-A

134177176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34049495-G-T

http://identifiers.org/hco/7/GRCh38#134177209-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#34049531-C-A

134177360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34049647-C-T

134177603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34049871-A-G

134177603-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34049871-A-T

134177699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34049934-A-G

134177720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34049955-T-C

134177803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34050030-A-G

http://identifiers.org/hco/7/GRCh38#134177809-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#34050036-A-C

134178066-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34050259-G-C

134178106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34050302-T-C

134178357-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34050517-G-T

134178378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34050537-T-C

134178378-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34050537-T-G

134178468-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34050616-T-A

134178468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34050616-T-C

134178625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34050773-C-T

http://identifiers.org/hco/7/GRCh38#134178633-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#34050781-C-A

134178633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34050781-C-T

http://identifiers.org/hco/7/GRCh38#134178676-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#34050847-C-A

134178676-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34050847-C-G

134178676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34050847-C-T

http://identifiers.org/hco/7/GRCh38#134178682-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#34050854-C-A

134178682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34050854-C-T

http://identifiers.org/hco/7/GRCh38#134178706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#34050878-C-A

http://identifiers.org/hco/7/GRCh38#134178707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#34050879-C-A

134178707-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34050879-C-G

134178709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34050881-A-G

134178709-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34050881-A-T

134178799-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34051539-T-A

134178865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34051597-T-C

http://identifiers.org/hco/7/GRCh38#134178954-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#34051674-A-C

134178954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34051674-A-G

134179064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34052499-C-T

134179253-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34052676-T-C

134179254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34052677-G-A

134179417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34052838-C-T

134181538-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34053573-G-T

134181639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34053639-A-G

134181654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34053656-T-C

134181708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34053710-A-G

134182037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34054010-A-G

134182042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34054015-T-C

134182408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34054348-G-A

134182560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34054465-C-T

134183057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34054789-C-T

http://identifiers.org/hco/7/GRCh38#134183666-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#34055378-A-C

134183666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34055378-A-G

134183719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34055553-G-A

134183758-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 34055623-T-G

134183794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 34055659-T-C

http://identifiers.org/hco/7/GRCh38#134183906-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#34055770-A-C

134183906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34055770-A-G

134183906-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34055770-A-T

134183927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34055795-A-G

134183927-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34055795-A-T

http://identifiers.org/hco/7/GRCh38#134183989-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#34055853-C-A

134183989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34055853-C-T

134184139-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34055987-C-G

134184211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34056060-T-C

134184800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34056289-G-A

134185677-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34057325-G-C

134185828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34057475-A-G

134186122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34057761-A-G

134186406-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34058024-G-T

http://identifiers.org/hco/7/GRCh38#134186425-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#34058043-C-A

134186757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34058370-A-G

134186853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34058456-G-A

134186853-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34058456-G-T

134186932-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34058521-C-G

134186932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34058521-C-T

134187278-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34058851-T-G

134187637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34059168-A-G

134187999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34059456-G-A

134188246-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34059683-T-G

134188652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34060463-C-T

134188723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34060532-G-A

134188745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34060554-A-G

134188777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34060611-G-T

134188847-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34060680-A-T

134188892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34060728-T-C

134188924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34060750-C-T

134189020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34060852-A-G

134189119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34060957-A-G

http://identifiers.org/hco/7/GRCh38#134189291-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#34061139-C-A

134189291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34061139-C-T

134189437-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34061307-G-C

134189467-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34061338-T-G

134190054-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34061902-T-A

134190170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34061961-C-T

134190540-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34062014-T-G

134190586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34062061-A-G

134190749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34062225-A-G

134191010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34062653-C-T

134191088-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34062731-T-G

134191599-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34063216-T-A

134191599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34063216-T-C

134191636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34063256-A-G

134191639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34063259-T-C

134191849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34063551-T-C

134191849-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34063551-T-G

http://identifiers.org/hco/7/GRCh38#134192559-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#34063643-C-A

http://identifiers.org/hco/7/GRCh38#134192610-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#34063684-C-A

134192652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34063728-A-G

134192748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34063805-G-A

134192781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34063838-A-G

134193006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34064012-T-C

134193361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34064361-A-G

134193429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34064430-C-T

134193560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34064562-C-T

134193601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34064603-T-C

134193827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34064815-C-T

134194062-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34065057-T-G

134194077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34065071-A-G

134195551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34065679-T-C

134195702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34065829-G-A

134195897-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34066014-G-T

134196069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34066220-T-C

134196715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34066848-A-G

http://identifiers.org/hco/7/GRCh38#134196820-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#34066939-C-A

134196824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34066943-G-A

134196842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34066955-G-A

134196842-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34066955-G-T

http://identifiers.org/hco/7/GRCh38#134197025-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#34067140-C-A

134197123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34067239-A-G

134197502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34067494-G-A

134197502-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34067494-G-T

134197648-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34067619-G-T

134197740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34067708-T-C

134198028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34067965-T-C

134198060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34067999-C-T

134198109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34068044-T-C

134198280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34068227-C-T

134198311-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34068324-G-C

134198317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34068330-A-G

134198319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34068332-C-T

134198490-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34068514-G-C

134198505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34068529-A-G

134198520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34068543-A-G

134198613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34068674-A-G

134198733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34068783-G-A

134198733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34068783-G-T

134198949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34069448-T-C

134198954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34069453-G-A

134199304-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 34069756-T-A

http://identifiers.org/hco/7/GRCh38#134199312-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#34069764-A-C

http://identifiers.org/hco/7/GRCh38#134199984-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#34071037-A-C

134199984-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34071037-A-T

134200028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34071079-A-G

134200028-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34071079-A-T

134200141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34071243-A-G

134200190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34071295-C-T

134200252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34071419-G-A

134200413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34071504-G-A

134200770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34071780-T-C

134200863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34071859-G-A

134201229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34072213-G-A

134201379-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34072358-T-A

134201417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34072395-T-C

134201417-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34072395-T-G

134201446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34072423-T-C

134201464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34072441-T-C

http://identifiers.org/hco/7/GRCh38#134201466-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#34072443-C-A

134201466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34072443-C-T

http://identifiers.org/hco/7/GRCh38#134201589-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#34072567-C-A

http://identifiers.org/hco/7/GRCh38#134201619-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#34072592-A-C

134201619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34072592-A-G

134201619-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34072592-A-T

http://identifiers.org/hco/7/GRCh38#134201632-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#34072605-C-A

134201632-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34072605-C-G

134201646-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34072616-T-A

134201695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34072669-T-C

134201695-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34072669-T-G

134202768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34073451-C-T

134203397-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34073566-G-C

134203650-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34073831-T-G

http://identifiers.org/hco/7/GRCh38#134203896-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
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#34073915-C-A

134203982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34074002-C-T

134204057-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34074078-T-A

134204162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34074163-C-T

134204218-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34074224-A-T

134204318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34074324-A-G

134204361-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34074367-G-T

134204362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34074368-C-T

http://identifiers.org/hco/7/GRCh38#134204713-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#34074723-C-A

134204738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34074748-C-T

134204831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34074839-A-G

134205463-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34075685-G-T

134205576-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34075867-A-T

134205652-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34075936-G-C

134205684-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34075968-G-C

134205782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34076079-G-A

134205909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34076222-A-G

134206830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34076929-G-A

134207336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34077565-A-G

134207340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34077569-C-T

134207485-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34077705-A-T

134207498-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34077718-C-G

134207521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34077741-T-C

134207634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34077853-C-T

134207646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34077865-G-A

134207872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34078031-C-T

http://identifiers.org/hco/7/GRCh38#134207877-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#34078036-A-C

134208064-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34078123-C-G

134208608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34078516-G-A

134208633-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34078542-G-T

134208837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 34078740-G-T

134208870-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 34078773-G-T

134208894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 34078797-A-G

134208960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 34078839-T-C

134208960-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 34078839-T-G

134209077-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 34078953-T-A

134209077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 34078953-T-C

http://identifiers.org/hco/7/GRCh38#134209114-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#34079002-A-C

134209114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 34079002-A-G

http://identifiers.org/hco/7/GRCh38#134209152-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#34079114-C-A

134209152-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 34079114-C-G

134209152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 34079114-C-T

134209167-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 34079145-T-A

134209167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 34079145-T-C

http://identifiers.org/hco/7/GRCh38#134209237-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#34079215-C-A

134209237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 34079215-C-T

134209252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 34079230-C-T

134209253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 34079231-C-T

134209277-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 34079255-T-A

134209292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 34079270-T-C

134209332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 34079310-T-C

http://identifiers.org/hco/7/GRCh38#134209372-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#34079347-C-A

http://identifiers.org/hco/7/GRCh38#134209557-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#34079517-C-A

http://identifiers.org/hco/7/GRCh38#134209631-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#34079591-C-A

http://identifiers.org/hco/7/GRCh38#134209726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#34079686-C-A

134209752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 34079712-G-A

134209752-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 34079712-G-T

134209759-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 34079719-C-G

134209759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 34079719-C-T

http://identifiers.org/hco/7/GRCh38#134209766-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#34079726-C-A

134209766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 34079726-C-T

134209784-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 34079744-T-A

134209784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 34079744-T-C

134209798-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 34079758-G-T

http://identifiers.org/hco/7/GRCh38#134209815-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#34079775-C-A

134209898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 34079858-G-A

134209898-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 34079858-G-C

134209898-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 34079858-G-T

134209936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 34079896-C-T

134209971-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 34079931-G-T

http://identifiers.org/hco/7/GRCh38#134209995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#34079955-C-A

134209995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 34079955-C-T

http://identifiers.org/hco/7/GRCh38#134210046-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#34080006-C-A

134210046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 34080006-C-T

134210081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 34080041-G-A

134210081-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 34080041-G-C

134210081-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 34080041-G-T

134210124-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 34080081-G-T

134210165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 34080122-C-T

134210384-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34080245-A-T

134210404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34080265-A-G

134210522-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34080368-C-G

134210529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34080375-T-C

134210545-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34080391-C-G

134210662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34080484-A-G

134210841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34080663-C-T

http://identifiers.org/hco/7/GRCh38#134210860-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#34080682-C-A

134210935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34080757-C-T

134211274-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34080989-G-T

134211401-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34081095-A-T

134211437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34081138-A-G

134211551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34081235-A-G

134211578-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34081261-T-C

134211634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34081314-T-C

134211680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34081353-T-C

134211807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34081474-G-T

134211931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34081603-A-G

134212001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34081676-C-T

134212252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34081926-T-C

134212325-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34081997-G-C

134212583-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34082255-A-T

134212605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34082277-T-C

134212763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34082412-G-A

134212781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34082423-G-A

134212950-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34082580-C-G

134213301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34082880-A-G

134213319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34082894-G-A

134213330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34082905-T-C

134213687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34083455-T-C

134213756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34083503-A-G

134214221-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34083935-T-G

134214344-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34084020-A-G

134214399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34084073-A-G

134214652-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34084302-T-A

134214926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34084467-A-G

134214969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34084500-A-G

134214971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34084502-A-G

134215270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34084798-A-G

134215270-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34084798-A-T

134215530-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34085027-T-A

134215530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34085027-T-C

134215646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34085162-T-C

134215667-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34085183-C-G

134215667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34085183-C-T

134216008-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34085508-C-G

134216026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34085526-T-C

134217095-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34086567-G-T

134217249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34086707-C-T

134217332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34086793-G-A

134217332-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34086793-G-T

134217921-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34087370-T-A

134218329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34087500-G-A

134218329-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34087500-G-C

134218400-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34087572-T-A

134218475-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34087615-G-C

134218559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34087698-A-G

134218698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34087832-A-G

134219690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34091192-C-T

134220055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34091557-T-C

134220172-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34091659-T-A

134220256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34091745-C-T

134220328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34091819-C-T

134220329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34091820-A-G

134220331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34091822-G-A

134220414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34091890-G-A

134220414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34091890-G-T

134221084-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34092479-T-A

134221200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34092595-G-A

134221332-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34092902-G-T

134221355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34092925-G-A

134221450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34092998-A-G

http://identifiers.org/hco/7/GRCh38#134221670-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#34093209-A-C

134221670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34093209-A-G

134221670-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34093209-A-T

134221672-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34093211-G-C

134221672-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34093211-G-T

134221682-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34093221-T-G

134221750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34093297-T-C

134221768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34093315-T-C

http://identifiers.org/hco/7/GRCh38#134221788-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#34093333-C-A

134221972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron variant
orthologous variants: 34093593-A-G

134222019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron variant
orthologous variants: 34093649-T-C

134222064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 34093700-T-C

134222222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 34093851-T-C

134222352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 34093959-C-T

134222422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 34094030-G-A

134245796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron variant
orthologous variants: 34102022-A-G

http://identifiers.org/hco/7/GRCh38#134246073-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#34102304-A-C

134246093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron variant
orthologous variants: 34102324-C-T

134246104-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron variant
orthologous variants: 34102335-G-T

134246715-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron variant
orthologous variants: 34102885-C-G

134246898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron variant
orthologous variants: 34103061-T-C

134247074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron variant
orthologous variants: 34103258-A-G

134247177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron variant
orthologous variants: 34103361-A-G

134247177-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron variant
orthologous variants: 34103361-A-T

134247226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron variant
orthologous variants: 34103394-T-C

http://identifiers.org/hco/7/GRCh38#134247487-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#34104046-A-C

134247487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron variant
orthologous variants: 34104046-A-G

134247600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: synonymous variant
orthologous variants: 34104156-T-C

134247684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron variant
orthologous variants: 34104252-T-C

134247834-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron variant
orthologous variants: 34104399-C-G

http://identifiers.org/hco/7/GRCh38#134247863-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#34104426-A-C

134247979-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron variant
orthologous variants: 34105180-T-A

134248063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron variant
orthologous variants: 34105252-A-G

134248203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron variant
orthologous variants: 34105390-C-T

http://identifiers.org/hco/7/GRCh38#134248397-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#34105572-C-A

134248442-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron variant
orthologous variants: 34105585-T-G

http://identifiers.org/hco/7/GRCh38#134248632-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#34105764-C-A

134248632-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron variant
orthologous variants: 34105764-C-G

134248713-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron variant
orthologous variants: 34105849-A-T

134248815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron variant
orthologous variants: 34105934-T-C

134248815-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron variant
orthologous variants: 34105934-T-G

134248860-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron variant
orthologous variants: 34105960-T-A

134248901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron variant
orthologous variants: 34106013-T-C

134248901-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron variant
orthologous variants: 34106013-T-G

134248918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron variant
orthologous variants: 34106030-G-A

134248918-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron variant
orthologous variants: 34106030-G-T

134249003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: missense variant
orthologous variants: 34106092-G-A

134249003-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: stop gained
orthologous variants: 34106092-G-T

134249029-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: synonymous variant
orthologous variants: 34106118-T-A

http://identifiers.org/hco/7/GRCh38#134249060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#34106149-C-A

http://identifiers.org/hco/7/GRCh38#134249066-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#34106155-C-A

134249094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron variant
orthologous variants: 34106197-G-A

134249094-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron variant
orthologous variants: 34106197-G-C

134249101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron variant
orthologous variants: 34106204-G-A

134249101-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron variant
orthologous variants: 34106204-G-C

134249105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron variant
orthologous variants: 34106208-T-C

134249338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron variant
orthologous variants: 34106407-C-T

http://identifiers.org/hco/7/GRCh38#134249601-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#34106914-C-A

134249602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron variant
orthologous variants: 34106915-A-G

134249680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron variant
orthologous variants: 34106975-A-G

134258072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron variant
orthologous variants: 34108738-A-G

134258116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron variant
orthologous variants: 34108768-A-G

134258125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron variant
orthologous variants: 34108777-A-G

134258127-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron variant
orthologous variants: 34108779-A-T

134258132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron variant
orthologous variants: 34108784-A-G

134258132-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron variant
orthologous variants: 34108784-A-T

134258151-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron variant
orthologous variants: 34108804-T-G

134258190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron variant
orthologous variants: 34108842-G-A

134258270-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: missense variant
orthologous variants: 34108910-T-G

134258359-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: missense variant
orthologous variants: 34109002-C-G

134258724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron variant
orthologous variants: 34109062-A-G

134258744-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron variant
orthologous variants: 34109080-G-T

134258852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron variant
orthologous variants: 34109157-C-T

http://identifiers.org/hco/7/GRCh38#134258990-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#34109284-C-A

134259139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 34109417-C-T

134259141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 34109419-C-T

134259146-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 34109427-C-G

134259358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 34109621-G-A

http://identifiers.org/hco/7/GRCh38#134263709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#34110139-C-A

134263729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron variant
orthologous variants: 34110164-T-C

134263830-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron variant
orthologous variants: 34110242-C-G

134263830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron variant
orthologous variants: 34110242-C-T

134263834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron variant
orthologous variants: 34110245-A-G

134263834-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron variant
orthologous variants: 34110245-A-T

134263836-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron variant
orthologous variants: 34110247-G-T

134263914-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron_variant, missense_variant
orthologous variants: 34110325-T-A

134263989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 34110431-G-A

134263989-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 34110431-G-C

http://identifiers.org/hco/7/GRCh38#134264280-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#34110680-C-A

134264280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 34110680-C-T

134264286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 34110684-G-A

134264286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 34110684-G-T

134264302-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 34110700-T-G

http://identifiers.org/hco/7/GRCh38#134264326-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#34110725-A-C

134264326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 34110725-A-G

http://identifiers.org/hco/7/GRCh38#134264500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#34110886-C-A

134264500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 34110886-C-T

http://identifiers.org/hco/7/GRCh38#134264561-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#34110938-C-A

134264867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21964
most severe consequence: intron variant
orthologous variants: 34111212-A-G