34844806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 155332390-G-A

34844806-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 155332390-G-T

34844846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 155332431-A-G

34845223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 155332769-G-A

34845223-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 155332769-G-C

34845223-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 155332769-G-T

34845518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 155333065-A-G

34845599-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 155333138-T-A

34845599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 155333138-T-C

34845661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 155333203-T-C

34845677-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 155333225-A-T

34849223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 155335028-C-T

34849356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 155335039-G-A

34849356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 155335039-G-T

http://identifiers.org/hco/20/GRCh38#34849630-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155335218-C-A

34849634-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 155335222-A-G

34849869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 155335440-T-C

34849884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 155335455-G-A

34849884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 155335455-G-T

http://identifiers.org/hco/20/GRCh38#34849922-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155335491-C-A

http://identifiers.org/hco/20/GRCh38#34849949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155335517-C-A

34849949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 155335517-C-T

34849965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 155335533-C-T

34850015-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155335583-G-C

http://identifiers.org/hco/20/GRCh38#34850193-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155335788-C-A

34850193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 155335788-C-T

34850291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 155335886-G-A

34850745-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 155336462-G-T

34850747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 155336464-G-A

34850756-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 155336473-T-A

34850756-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 155336473-T-G

http://identifiers.org/hco/20/GRCh38#34850784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155336491-C-A

34850784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 155336491-C-T

34850813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 155336518-T-C

34850813-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 155336518-T-G

34850846-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 155336551-A-T

http://identifiers.org/hco/20/GRCh38#34851119-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155336663-C-A

http://identifiers.org/hco/20/GRCh38#34851143-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155336687-A-C

34851143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 155336687-A-G

34851398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 155336933-G-A

34851422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 155336954-G-A

34851422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 155336954-G-T

34851456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 155336985-C-T

34851517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 155337043-A-G

http://identifiers.org/hco/20/GRCh38#34851525-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155337051-A-C

34851827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 155337323-A-G

34851856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 155337352-G-A

34851911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 155337391-C-T

34851941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 155337420-C-T

34851968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 155337425-G-A

http://identifiers.org/hco/20/GRCh38#34852086-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155337496-C-A

34852086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 155337496-C-T

http://identifiers.org/hco/20/GRCh38#34852091-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155337501-A-C

http://identifiers.org/hco/20/GRCh38#34852108-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155337518-A-C

34852108-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 155337518-A-T

34852158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 155337565-G-A

34852158-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155337565-G-C

34852158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155337565-G-T

http://identifiers.org/hco/20/GRCh38#34852309-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155337713-A-C

34852309-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 155337713-A-T

34852331-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 155337735-C-G

34852331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 155337735-C-T

34852333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 155337737-C-T

34852454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 155337859-G-A

34852454-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155337859-G-C

34852526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 155337931-G-A

http://identifiers.org/hco/20/GRCh38#34852570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155337975-C-A

34852570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155337975-C-T

http://identifiers.org/hco/20/GRCh38#34852588-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155337993-C-A

34852588-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155337993-C-G

34852588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155337993-C-T

34852647-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155338045-A-T

34852670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155338075-G-A

34852670-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155338075-G-T

http://identifiers.org/hco/20/GRCh38#34852885-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155338278-A-C

34854294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155340470-T-C

34854299-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155340479-G-C

34854627-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 155340779-T-G

34854636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155340788-G-T

http://identifiers.org/hco/20/GRCh38#34854657-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155340808-C-A

34854657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155340808-C-T

34854952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155341091-G-A

http://identifiers.org/hco/20/GRCh38#34854970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155341109-C-A

34854970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155341109-C-T

34854977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155341116-T-C

34854995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155341133-C-T

34855056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155341167-A-G

34855056-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155341167-A-T

34855174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155341239-A-G

34855487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155341577-T-C

34855529-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155341642-C-G

34855668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155341790-C-T

34856395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155342151-G-A

34856427-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155342182-A-T

34856445-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155342194-G-C

34856467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155342217-C-T

34856684-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155342500-G-T

http://identifiers.org/hco/20/GRCh38#34856686-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155342502-A-C

34856754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155342570-G-A

34856754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155342570-G-T

34856835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155342652-A-G

34856839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155342656-G-A

34856839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155342656-G-T

34856879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 155342696-C-T

34856910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155342719-G-A

34856910-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155342719-G-C

34856910-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155342719-G-T

34856932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155342741-G-A

34856932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155342741-G-T

34856941-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155342750-T-G

http://identifiers.org/hco/20/GRCh38#34856956-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155342765-A-C

34856956-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155342765-A-T

34856997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155342802-G-A

34856997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155342802-G-T

34857399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155343556-C-T

34857474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155343610-G-A

34857474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155343610-G-T

http://identifiers.org/hco/20/GRCh38#34859390-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155344528-C-A

34859477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155344590-G-A

34859477-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155344590-G-T

34859568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155344681-G-A

34859568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155344681-G-T

http://identifiers.org/hco/20/GRCh38#34859629-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155344742-C-A

34859629-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 155344742-C-G

34859629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 155344742-C-T

http://identifiers.org/hco/20/GRCh38#34859747-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155344846-C-A

34859747-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155344846-C-G

34859747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155344846-C-T

34859836-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155344931-T-A

34859836-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155344931-T-G

http://identifiers.org/hco/20/GRCh38#34859858-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155344939-C-A

http://identifiers.org/hco/20/GRCh38#34859920-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155344992-C-A

34859920-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155344992-C-G

34859938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155345010-T-C

34859939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155345011-G-A

34859939-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155345011-G-T

34860015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 155345094-A-G

http://identifiers.org/hco/20/GRCh38#34860077-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155345156-C-A

34860077-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 155345156-C-G

34860077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 155345156-C-T

34860129-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 155345208-T-A

34860129-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 155345208-T-G

34860229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155345308-T-C

34860232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155345311-T-C

34860417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155345496-G-A

34860453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155345532-G-A

34860453-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155345532-G-C

34860453-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155345532-G-T

34860591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155345672-C-T

34860616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155345697-T-C

34860994-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155345800-G-T

34861349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155346523-T-C

34861390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155346564-G-A

34861390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155346564-G-T

34861469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 155346648-G-A

34861469-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 155346648-G-T

34861597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155346774-A-G

http://identifiers.org/hco/20/GRCh38#34861605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155346782-C-A

34861605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155346782-C-T

34862058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155347161-G-A

34862175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155347257-T-C

34862527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155347598-C-T

34862698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155347748-G-T

34862741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155347786-T-C

http://identifiers.org/hco/20/GRCh38#34862759-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155347804-C-A

34862759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155347804-C-T

34862928-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155347989-C-G

34862928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155347989-C-T

34862929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155347990-G-A

34862929-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155347990-G-C

http://identifiers.org/hco/20/GRCh38#34863004-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155348058-C-A

http://identifiers.org/hco/20/GRCh38#34863024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155348076-C-A

34863024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155348076-C-T

http://identifiers.org/hco/20/GRCh38#34863075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155348103-C-A

34863075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155348103-C-T

34863210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155348172-T-C

34863361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 155348294-G-A

34863361-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 155348294-G-C

http://identifiers.org/hco/20/GRCh38#34863552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155348485-C-A

34863552-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 155348485-C-G

34863552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 155348485-C-T

34863575-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155348509-T-A

34863611-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155348544-T-G

34863623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155348556-G-A

http://identifiers.org/hco/20/GRCh38#34863718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155348647-C-A

34863725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 155348654-G-A

http://identifiers.org/hco/20/GRCh38#34863726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155348655-C-A

34863726-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 155348655-C-G

34863726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 155348655-C-T

34863792-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 155348712-T-A

34863792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 155348712-T-C

http://identifiers.org/hco/20/GRCh38#34863816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155348735-C-A

34863816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 155348735-C-T

34863829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 155348748-G-A

34863829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 155348748-G-T

34863965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 155348871-C-T

34866066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155350751-T-C

34869483-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155353994-G-C

34869703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155354191-G-A

34869799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155354293-T-C

34870295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155354795-C-T

34870298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155354798-G-A

34870326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155354875-C-T

34871313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155355202-T-C

http://identifiers.org/hco/20/GRCh38#34871505-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155355413-C-A

34871621-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155355499-G-C

34871750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155355634-G-A

34871935-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155355817-C-G

34871965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155355844-G-A

34872267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155356155-T-C

http://identifiers.org/hco/20/GRCh38#34872300-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155356187-C-A

34872348-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155356235-T-G

http://identifiers.org/hco/20/GRCh38#34872463-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155356349-C-A

34872463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4259
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155356349-C-T