http://identifiers.org/hco/11/GRCh38#117800974-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45336881-C-A

http://identifiers.org/hco/11/GRCh38#117801376-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45336515-C-A

http://identifiers.org/hco/11/GRCh38#117801383-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45336508-C-A

117801440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45336431-T-C

http://identifiers.org/hco/11/GRCh38#117801522-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45336222-C-A

117801523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45336221-T-C

117801753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45336031-G-A

117801753-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45336031-G-T

http://identifiers.org/hco/11/GRCh38#117801759-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45336025-C-A

117801822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45335965-A-G

117801848-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45335945-G-T

117801911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45335906-A-G

117801989-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45335835-A-T

http://identifiers.org/hco/11/GRCh38#117802005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45335819-C-A

http://identifiers.org/hco/11/GRCh38#117802134-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45335710-C-A

117802156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45335689-T-C

117802353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45334457-G-A

117802557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45334283-G-A

117802602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45334238-T-C

117802620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45334220-A-G

117802650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45334190-C-T

http://identifiers.org/hco/11/GRCh38#117802744-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45334090-A-C

117802744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45334090-A-G

117803832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45332504-G-A

117803914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45332436-T-C

http://identifiers.org/hco/11/GRCh38#117803930-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45332420-A-C

117803978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45332372-T-C

117803997-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45332353-T-A

117804010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45332340-G-A

117804499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45331959-C-T

117806124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45330105-C-T

117806179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45330050-G-A

117806268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45329964-C-T

117806459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45329802-T-C

117806459-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45329802-T-G

117806677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45329603-G-A

117807124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45329190-T-C

117807200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45329126-T-C

117807249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45329081-T-C

117807365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45328965-A-G

117807434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45328898-C-T

117807482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45328851-C-T

117807558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45328807-A-G

117807715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45328714-C-T

117808107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45328589-A-G

117808188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45328532-G-A

117808467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45328255-C-T

117808665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45328016-A-G

117808917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45327826-C-T

117808949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45327794-G-A

117808953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45327790-C-T

http://identifiers.org/hco/11/GRCh38#117809480-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#45327386-C-A

117809514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45327352-C-T

117809566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45327316-A-G

117809705-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45327199-G-C

117814803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45325062-G-A

117815069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45324808-T-C

117815108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45324772-C-T

117815413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45324516-G-A

117815445-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45324480-T-C

117815448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45324477-G-A

117815562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45324371-G-A

117815943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45324189-G-A

http://identifiers.org/hco/11/GRCh38#117815944-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45324188-C-A

117815944-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45324188-C-G

117815946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45324186-G-A

117816328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45323895-A-G

117816410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45323854-G-A

117816549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45323772-A-G

117816556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45323766-C-T

117816620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45323717-G-A

117816620-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45323717-G-T

117816808-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45323599-G-C

117817845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45323318-C-T

117817857-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45323306-T-A

117817860-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45323303-G-C

http://identifiers.org/hco/11/GRCh38#117818082-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#45323090-C-A

117818082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45323090-C-T

117818137-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45323045-G-T

117818199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45322973-A-G

117818199-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45322973-A-T

117818272-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45322916-G-T

117818361-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45322805-G-T

http://identifiers.org/hco/11/GRCh38#117818428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#45322732-C-A

117818428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45322732-C-T

117818497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45322662-T-C

http://identifiers.org/hco/11/GRCh38#117818542-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45322616-C-A

117818596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45322561-G-A

117818596-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45322561-G-T

http://identifiers.org/hco/11/GRCh38#117818678-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45322511-C-A

http://identifiers.org/hco/11/GRCh38#117818779-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45322433-C-A

117818779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45322433-C-T

117819077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45322292-G-A

117819077-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45322292-G-T

117819080-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45322289-G-T

117819092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 45322273-G-T

117819112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45322254-A-G

117819141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 45322225-G-A

117819141-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 45322225-G-T

http://identifiers.org/hco/11/GRCh38#117819247-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#45322144-C-A

117819521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45322018-G-T

117819552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45321987-C-T

117819670-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45321880-G-T

117819684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45321874-A-G

117819687-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45321871-T-G

117819829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45321755-G-A

117819829-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45321755-G-C

117819834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45321750-G-A

117819928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45321647-G-A

117820011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45321567-A-G

117820056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45321526-A-G

http://identifiers.org/hco/11/GRCh38#117820336-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45321324-C-A

117820338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45321322-A-G

117820339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45321321-G-A

117820354-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45321306-G-C

117820395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45321264-G-A

117820395-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45321264-G-T

http://identifiers.org/hco/11/GRCh38#117820442-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45321222-C-A

117820442-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45321222-C-G

117820442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45321222-C-T

117820472-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45321188-G-T

117820512-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45321147-T-C

http://identifiers.org/hco/11/GRCh38#117820540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45321120-C-A

117820614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45321078-T-C

117820637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45321052-C-T

117820752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45320948-G-A

117820799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45320900-C-T

117820835-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45320867-T-A

117820848-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45320856-G-T

http://identifiers.org/hco/11/GRCh38#117820881-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45320823-A-C

117820881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45320823-A-G

117821189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45320705-T-C

117821192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45320702-G-A

http://identifiers.org/hco/11/GRCh38#117821449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45320615-C-A

117821449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45320615-C-T

117821450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45320614-G-A

117821450-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45320614-G-C

117821450-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45320614-G-T

http://identifiers.org/hco/11/GRCh38#117821477-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45320587-C-A

117821493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45320572-A-G

http://identifiers.org/hco/11/GRCh38#117821705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45320480-C-A

http://identifiers.org/hco/11/GRCh38#117821707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45320478-C-A

117821707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45320478-C-T

117821709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45320476-C-T

117821720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45320464-C-T

117821776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45320445-G-A

117821776-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45320445-G-T

117821786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45320435-G-A

117821855-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45320365-T-G

117821865-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45320355-G-C

http://identifiers.org/hco/11/GRCh38#117821914-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45320320-A-C

117821914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45320320-A-G

117821935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45320298-G-A

117821935-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45320298-G-C

117821935-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45320298-G-T

117821964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45320269-C-T

117821997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45320236-G-A

117821997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45320236-G-T

117822050-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45320180-G-C

117822050-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45320180-G-T

http://identifiers.org/hco/11/GRCh38#117822094-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45320124-C-A

117822094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45320124-C-T

117822106-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45320105-G-T

117822122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45320095-C-T

117822135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45320082-T-C

117822262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45319842-C-T

117822370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45319724-G-A

117822370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45319724-G-T

117822411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45319665-A-G

117822468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45319608-A-G

117822490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45319587-G-T

117822520-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45319557-T-A

http://identifiers.org/hco/11/GRCh38#117822521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45319556-C-A

117822521-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45319556-C-G

http://identifiers.org/hco/11/GRCh38#117822552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45319531-C-A

117822552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45319531-C-T

117822575-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45319516-G-C

117822575-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45319516-G-T

117822576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45319515-G-A

117822576-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45319515-G-C

117822642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45319470-G-A

117822642-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45319470-G-C

117822642-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45319470-G-T

117822698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45319421-G-A

117822810-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45319326-G-T

http://identifiers.org/hco/11/GRCh38#117822812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45319324-C-A

117822812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45319324-C-T

117822821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45319315-G-A

http://identifiers.org/hco/11/GRCh38#117822863-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45319261-A-C

117823166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45318981-G-A

117823408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45318732-C-T

117823579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45318563-C-T

117823753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45318382-C-T

117824016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45318145-G-A

http://identifiers.org/hco/11/GRCh38#117824052-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45318116-C-A

http://identifiers.org/hco/11/GRCh38#117824063-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45318105-C-A

117824063-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45318105-C-G

http://identifiers.org/hco/11/GRCh38#117824070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45318104-C-A

http://identifiers.org/hco/11/GRCh38#117824074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45318100-C-A

117824074-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45318100-C-G

http://identifiers.org/hco/11/GRCh38#117824094-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45318083-C-A

117824141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45318045-T-C

117824167-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45318018-T-A

117824167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45318018-T-C

http://identifiers.org/hco/11/GRCh38#117824208-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45317956-C-A

117824208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45317956-C-T

117824209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45317955-T-C

117824241-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45317926-A-T

117824475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45317585-G-A

117824475-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45317585-G-T

http://identifiers.org/hco/11/GRCh38#117824829-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45317298-A-C

117824879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron variant
orthologous variants: 45317245-G-A

117824879-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron variant
orthologous variants: 45317245-G-C

117824879-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron variant
orthologous variants: 45317245-G-T

117825135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron variant
orthologous variants: 45316981-G-A

117825406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron variant
orthologous variants: 45316708-C-T

117825452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron variant
orthologous variants: 45316695-C-T

117825489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron variant
orthologous variants: 45316671-C-T

117825553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron variant
orthologous variants: 45316608-C-T

117825607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron variant
orthologous variants: 45316565-A-G

117826110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron variant
orthologous variants: 45315666-T-C

117826374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron variant
orthologous variants: 45315442-G-A

117826374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron variant
orthologous variants: 45315442-G-T

117826597-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron variant
orthologous variants: 45315232-T-G

117827708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron variant
orthologous variants: 45314815-A-G

117827708-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron variant
orthologous variants: 45314815-A-T

117827918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron variant
orthologous variants: 45314672-G-A

117827918-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron variant
orthologous variants: 45314672-G-C

117827918-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron variant
orthologous variants: 45314672-G-T

117827932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron variant
orthologous variants: 45314658-G-T

http://identifiers.org/hco/11/GRCh38#117827933-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45314657-A-C

117827933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron variant
orthologous variants: 45314657-A-G

117827963-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron variant
orthologous variants: 45314629-C-G

117827963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron variant
orthologous variants: 45314629-C-T

http://identifiers.org/hco/11/GRCh38#117827996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, splice_region_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45314595-C-A

117828078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 45314511-T-C

117828078-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 45314511-T-G

117828181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron variant
orthologous variants: 45314408-G-A

117828181-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron variant
orthologous variants: 45314408-G-T

117828448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron_variant, undefined
orthologous variants: 45314117-T-C

117828498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4026
most severe consequence: intron variant
orthologous variants: 45314068-G-A