129434455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29917048-G-A

129434455-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29917048-G-C

129434455-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29917048-G-T

http://identifiers.org/hco/7/GRCh38#129434458-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29917051-C-A

129434458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29917051-C-T

http://identifiers.org/hco/7/GRCh38#129434571-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#29917199-A-C

129434571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 29917199-A-G

http://identifiers.org/hco/7/GRCh38#129434643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#29917250-C-A

129434643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29917250-C-T

129434654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29917261-A-G

129434832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29917351-T-C

129435016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29917509-T-C

129435968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29918743-A-G

129436121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29918850-G-A

129436416-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29919201-T-G

129436652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29919405-G-A

129436710-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29919457-G-C

http://identifiers.org/hco/7/GRCh38#129436748-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29919492-A-C

129439944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29920394-T-C

129439955-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29920405-A-T

http://identifiers.org/hco/7/GRCh38#129440162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29920605-C-A

129440162-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29920605-C-G

129440173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29920616-T-C

129440207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29920649-G-A

129440207-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29920649-G-T

129440209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29920651-T-C

129440236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29920680-A-G

129440246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29920685-T-C

129440547-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29920939-C-G

129440547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29920939-C-T

129440583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29920974-A-G

129440739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29921129-G-A

129440866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29921257-T-C

129442670-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29922980-T-A

129442779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29923090-A-G

129443923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29923817-G-A

129443936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29923830-G-A

http://identifiers.org/hco/7/GRCh38#129443957-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29923851-C-A

129443979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29923872-T-C

129443981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29923874-T-C

129443981-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29923874-T-G

129443997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29923888-G-A

129444157-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29924059-G-C

129444157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29924059-G-T

129444183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29924085-G-A

129444183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29924085-G-T

http://identifiers.org/hco/7/GRCh38#129444195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29924097-C-A

129444195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29924097-C-T

129450446-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29924271-T-G

129450456-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29924281-C-G

129451488-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29924758-G-T

129451760-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29925115-C-G

129451760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29925115-C-T

http://identifiers.org/hco/7/GRCh38#129451892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29925227-C-A

129451892-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29925227-C-G

129452434-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29925730-G-T

129452494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29925780-G-A

129452494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29925780-G-T

129452948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29926077-G-A

http://identifiers.org/hco/7/GRCh38#129453106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29926433-C-A

129453106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29926433-C-T

129453185-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29926508-C-G

129453213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29926542-G-A

129453215-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29926544-C-G

129453276-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 29926605-G-C

http://identifiers.org/hco/7/GRCh38#129453333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29926662-C-A

129453362-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29926691-G-C

129453401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29926722-G-A

129453401-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29926722-G-C

129453401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29926722-G-T

http://identifiers.org/hco/7/GRCh38#129453441-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29926744-C-A

129453441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29926744-C-T

129454032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29927212-G-A

129454032-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29927212-G-T

129454093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29927271-G-A

129454093-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29927271-G-T

http://identifiers.org/hco/7/GRCh38#129454132-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29927309-C-A

129454132-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29927309-C-G

129454132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29927309-C-T

129454259-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29927434-T-A

129454364-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29927529-G-C

129454374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29927539-G-A

129454374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29927539-G-T

129454401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29927566-T-C

129454546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29927711-G-A

129454576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29927743-G-A

129454576-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29927743-G-T

129454601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29927764-G-A

http://identifiers.org/hco/7/GRCh38#129454665-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29927856-C-A

129454665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29927856-C-T

129454921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29928100-T-C

129455059-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29928248-G-T

129455140-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29928333-G-T

129455141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29928334-G-A

129455141-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29928334-G-T

http://identifiers.org/hco/7/GRCh38#129455175-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29928369-A-C

http://identifiers.org/hco/7/GRCh38#129455213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29928406-C-A

129455377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29928567-T-C

129455559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29928724-A-G

129455672-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29928837-A-T

129456145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29929280-T-C

129456149-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29929284-T-A

129456172-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29929307-G-C

129456375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29929509-A-G

129456384-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29929531-C-G

http://identifiers.org/hco/7/GRCh38#129456510-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29929850-A-C

129456510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 29929850-A-G

129456561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 29929901-G-A

129456600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 29929940-A-G

129456698-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29930046-T-A

129456718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29930066-G-A

129456718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29930066-G-T

129456758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29930096-G-A

129456758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29930096-G-T

129457723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29930656-C-T

129457890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29930825-A-G

129458051-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29930988-G-C

129458069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29931005-A-G

129458076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29931012-G-A

129458076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29931012-G-T

129458119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 29931055-C-T

129458165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 29931085-T-C

http://identifiers.org/hco/7/GRCh38#129458167-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29931087-C-A

129458167-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 29931087-C-G

129458167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 29931087-C-T

129458295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 29931199-G-A

http://identifiers.org/hco/7/GRCh38#129458464-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29931368-C-A

129458464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29931368-C-T

129458625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29931650-G-A

129458625-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29931650-G-T

129458701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29931752-C-T

129459487-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29932172-T-G

129459505-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29932190-G-C

129459660-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29932346-T-A

129459661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29932347-G-A

129459662-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29932348-G-T

129459720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29932401-A-G

129459866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29932538-C-T

http://identifiers.org/hco/7/GRCh38#129460250-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29932938-A-C

http://identifiers.org/hco/7/GRCh38#129460509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29933172-C-A

129460615-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29933374-G-T

129460616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29933375-A-G

129460616-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29933375-A-T

129460659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29933446-G-A

129460678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29933556-G-A

129460678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29933556-G-T

129460833-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29933885-C-G

129460833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29933885-C-T

http://identifiers.org/hco/7/GRCh38#129460863-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29933913-A-C

129461036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29934094-A-G

129461157-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29934214-G-C

129461603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29934638-A-G

129461958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29936534-G-A

129461967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29936543-T-C

129461991-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29936566-C-G

129462164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29936690-C-T

129462192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29936718-C-T

129462224-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29936749-T-G

129462495-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29936944-G-C

http://identifiers.org/hco/7/GRCh38#129462829-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29937446-A-C

http://identifiers.org/hco/7/GRCh38#129462936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29937553-C-A

129462936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29937553-C-T

129462989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 29937603-G-A

129462989-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 29937603-G-T

129462992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 29937606-A-G

129463286-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron variant
orthologous variants: 29937817-A-T

http://identifiers.org/hco/7/GRCh38#129463402-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29937926-A-C

129463988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron variant
orthologous variants: 29938405-A-G

129463988-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron variant
orthologous variants: 29938405-A-T

129463999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron variant
orthologous variants: 29938416-G-A

http://identifiers.org/hco/7/GRCh38#129464210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29938591-C-A

129464210-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron variant
orthologous variants: 29938591-C-G

129464512-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron variant
orthologous variants: 29938871-G-T

129464592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron variant
orthologous variants: 29939016-A-G

129464755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron variant
orthologous variants: 29939179-A-G

129464755-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron variant
orthologous variants: 29939179-A-T

http://identifiers.org/hco/7/GRCh38#129464850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29939263-C-A

129465194-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron variant
orthologous variants: 29939572-T-G

129465507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron variant
orthologous variants: 29939858-C-T

129465556-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron variant
orthologous variants: 29939899-C-G

http://identifiers.org/hco/7/GRCh38#129465763-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29940268-A-C

129465775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron variant
orthologous variants: 29940281-C-T

129465924-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron variant
orthologous variants: 29940417-T-G

129466417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron variant
orthologous variants: 29940756-C-T

129466936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron variant
orthologous variants: 29941212-G-A

129466961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron variant
orthologous variants: 29941237-C-T

129467246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron variant
orthologous variants: 29941727-T-C

129467246-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron variant
orthologous variants: 29941727-T-G

129467252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron variant
orthologous variants: 29941733-G-A

129467252-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron variant
orthologous variants: 29941733-G-T

129470171-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron variant
orthologous variants: 29943949-G-C

129470242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron variant
orthologous variants: 29944020-A-G

129470435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron variant
orthologous variants: 29944216-G-A

http://identifiers.org/hco/7/GRCh38#129470789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29944564-C-A

129470789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron variant
orthologous variants: 29944564-C-T

129470814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron variant
orthologous variants: 29944589-G-A

129470814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron variant
orthologous variants: 29944589-G-T

129471239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron variant
orthologous variants: 29944988-G-A

129472240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron variant
orthologous variants: 29946511-C-T

129472619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron variant
orthologous variants: 29946838-G-A

129480493-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 29952802-G-T

http://identifiers.org/hco/7/GRCh38#129480507-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29952815-A-C

129480652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 29953224-G-A

129480700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 29953267-A-G

129480700-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 29953267-A-T

129480790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 29953353-T-C

129480790-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 29953353-T-G

129480947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron variant
orthologous variants: 29953502-A-G

129480947-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron variant
orthologous variants: 29953502-A-T

129480965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron variant
orthologous variants: 29953519-G-A

129481190-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron variant
orthologous variants: 29953734-C-G

129482976-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, missense_variant
orthologous variants: 29955565-C-G

129483042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 29955631-G-A

129483042-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 29955631-G-T

http://identifiers.org/hco/7/GRCh38#129485443-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29956536-C-A

http://identifiers.org/hco/7/GRCh38#129485490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29956568-C-A

129485501-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron variant
orthologous variants: 29956579-T-A

129485501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron variant
orthologous variants: 29956579-T-C

129485501-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron variant
orthologous variants: 29956579-T-G

129485521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron variant
orthologous variants: 29956599-G-A

129485521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron variant
orthologous variants: 29956599-G-T

129485533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron variant
orthologous variants: 29956609-A-G

129485572-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 29956650-A-T

129485592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: missense_variant, synonymous_variant
orthologous variants: 29956670-A-G

129485646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 29956724-T-C

129485871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: 3 prime UTR variant
orthologous variants: 29956943-C-T

129485938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: 3 prime UTR variant
orthologous variants: 29957073-G-A

129485938-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: 3 prime UTR variant
orthologous variants: 29957073-G-T

http://identifiers.org/hco/7/GRCh38#129485948-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29957083-C-A

129485948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: 3 prime UTR variant
orthologous variants: 29957083-C-T

129485975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: 3 prime UTR variant
orthologous variants: 29957111-G-A

129485975-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: 3 prime UTR variant
orthologous variants: 29957111-G-T

129486015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: 3 prime UTR variant
orthologous variants: 29957151-G-T

129486053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: 3 prime UTR variant
orthologous variants: 29957188-T-C

129486327-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: 3 prime UTR variant
orthologous variants: 29957450-G-T

129486442-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: 3 prime UTR variant
orthologous variants: 29957548-T-A

129486442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: 3 prime UTR variant
orthologous variants: 29957548-T-C

129486491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: 3 prime UTR variant
orthologous variants: 29957597-G-A

129486491-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: 3 prime UTR variant
orthologous variants: 29957597-G-C

129486535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: 3 prime UTR variant
orthologous variants: 29957641-A-G

129486573-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: 3 prime UTR variant
orthologous variants: 29957674-G-T

129486611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: 3 prime UTR variant
orthologous variants: 29958309-A-G

129487571-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: 3 prime UTR variant
orthologous variants: 29958976-T-A

129487600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: 3 prime UTR variant
orthologous variants: 29959008-A-G

129487916-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: 3 prime UTR variant
orthologous variants: 29959314-C-G

129487953-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: 3 prime UTR variant
orthologous variants: 29959345-G-C

129487953-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: 3 prime UTR variant
orthologous variants: 29959345-G-T

129488026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: 3 prime UTR variant
orthologous variants: 29959418-C-T

129488075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: 3 prime UTR variant
orthologous variants: 29959466-T-C

129488216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22209
most severe consequence: 3 prime UTR variant
orthologous variants: 29959495-T-C