46267995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 85716540-G-A

46267995-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 85716540-G-T

46268015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 85716565-G-A

46268015-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 85716565-G-C

46268015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 85716565-G-T

http://identifiers.org/hco/22/GRCh38#46268016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85716566-C-A

46268016-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 85716566-C-G

46268016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 85716566-C-T

http://identifiers.org/hco/22/GRCh38#46268045-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#85716593-C-A

46268045-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 85716593-C-G

46268045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 85716593-C-T

http://identifiers.org/hco/22/GRCh38#46268066-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85716614-C-A

46268066-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 85716614-C-G

46268066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 85716614-C-T

http://identifiers.org/hco/22/GRCh38#46268100-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85716645-C-A

46268100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85716645-C-T

46268506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 85717342-G-A

46268537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 85717371-G-A

46268537-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 85717371-G-T

46271882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85718429-T-C

46272464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85718787-G-A

46272464-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85718787-G-C

46272464-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85718787-G-T

46272487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85718810-G-A

46272487-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85718810-G-C

46272487-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85718810-G-T

46272489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85718812-G-A

46272489-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85718812-G-C

46272489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85718812-G-T

46272510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85718838-G-A

46272510-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85718838-G-T

http://identifiers.org/hco/22/GRCh38#46272565-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85718891-A-C

46272565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85718891-A-G

46272939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85719455-C-T

46273392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85719769-G-A

46273688-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85720044-C-G

46273749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85720104-G-A

46273749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85720104-G-T

46273769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85720123-T-C

46273821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85720163-G-A

http://identifiers.org/hco/22/GRCh38#46273877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85720200-C-A

46273877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85720200-C-T

46273932-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 85720255-G-C

46273932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 85720255-G-T

46274118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85720424-G-A

46274118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85720424-G-T

46274119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85720425-G-A

46274119-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85720425-G-T

46274121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85720427-A-G

46274121-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85720427-A-T

46274133-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85720430-T-A

46274133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85720430-T-C

46274133-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85720430-T-G

http://identifiers.org/hco/22/GRCh38#46274135-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85720432-C-A

46274135-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85720432-C-G

46274135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85720432-C-T

46274158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85720434-G-A

46274158-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85720434-G-C

46274158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85720434-G-T

46274164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85720440-G-A

46274164-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85720440-G-C

46274164-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85720440-G-T

46274187-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85720451-T-G

http://identifiers.org/hco/22/GRCh38#46274189-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85720453-C-A

46274189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85720453-C-T

46274262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85720515-G-A

http://identifiers.org/hco/22/GRCh38#46274291-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85720544-C-A

http://identifiers.org/hco/22/GRCh38#46275187-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85722863-C-A

46275187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85722863-C-T

http://identifiers.org/hco/22/GRCh38#46275191-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85722867-C-A

46275191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85722867-C-T

46275211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85722887-T-C

http://identifiers.org/hco/22/GRCh38#46275430-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85723089-C-A

46275430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85723089-C-T

46275434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85723093-T-C

http://identifiers.org/hco/22/GRCh38#46275523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85723182-C-A

46278370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85725466-C-T

46278421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85725514-G-A

46278421-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85725514-G-T

http://identifiers.org/hco/22/GRCh38#46278451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85725535-C-A

46278451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85725535-C-T

http://identifiers.org/hco/22/GRCh38#46278459-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85725543-C-A

46278459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85725543-C-T

46278664-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85725744-A-T

46278688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85725768-G-A

46278688-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85725768-G-C

http://identifiers.org/hco/22/GRCh38#46278695-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85725775-C-A

46278695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85725775-C-T

46278757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85725814-G-A

46278757-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85725814-G-T

46278764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85725821-A-G

46278764-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85725821-A-T

46278770-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85725827-G-C

46278772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85725829-T-C

46279103-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85726190-C-G

46279271-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85726460-C-G

46279646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85726820-T-C

46280004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85727186-G-A

46280010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85727192-G-A

46280010-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85727192-G-T

http://identifiers.org/hco/22/GRCh38#46280215-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85727338-C-A

46280215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 85727338-C-T

46280312-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 85727371-G-T

46280336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 85727391-G-A

46280614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 85727571-A-G

46280660-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 85727610-C-G

46280660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 85727610-C-T

46280918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 85727849-T-C

46281049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 85727957-G-T

46281102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 85728013-C-T

46281354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 85728408-G-A

46281393-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 85728453-T-G

46281406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 85728466-C-T

46281463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 85728561-T-C

46281549-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 85728607-G-C

46281582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 85728638-C-T

46281584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 85728640-C-T

46281610-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 85728664-T-G

http://identifiers.org/hco/22/GRCh38#46281622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85728676-C-A

46281622-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 85728676-C-G

46281622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 85728676-C-T

46281709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 85728763-C-T

46281788-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85728846-T-A

46284012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 85730571-G-T

46285085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: intron variant
orthologous variants: 85731708-C-T

46285086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: intron variant
orthologous variants: 85731709-G-A

46285143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: intron variant
orthologous variants: 85731739-T-C

46285148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: intron variant
orthologous variants: 85731744-T-C

http://identifiers.org/hco/22/GRCh38#46285314-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85731908-A-C

46285315-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: intron variant
orthologous variants: 85731909-G-T

http://identifiers.org/hco/22/GRCh38#46285335-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85731928-A-C

46285335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: intron variant
orthologous variants: 85731928-A-G

46286690-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: intron variant
orthologous variants: 85735243-T-A

46286690-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: intron variant
orthologous variants: 85735243-T-G

46286819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: intron variant
orthologous variants: 85735355-G-A

http://identifiers.org/hco/22/GRCh38#46286957-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85735596-C-A

46286957-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: intron variant
orthologous variants: 85735596-C-G

46286957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: intron variant
orthologous variants: 85735596-C-T

http://identifiers.org/hco/22/GRCh38#46286980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85735619-C-A

46286980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: intron variant
orthologous variants: 85735619-C-T

http://identifiers.org/hco/22/GRCh38#46286990-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85735631-C-A

46286990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: intron variant
orthologous variants: 85735631-C-T

http://identifiers.org/hco/22/GRCh38#46287075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85735720-C-A

46287179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: intron variant
orthologous variants: 85735810-G-A

46287179-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: intron variant
orthologous variants: 85735810-G-T

http://identifiers.org/hco/22/GRCh38#46287180-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85735811-C-A

46287180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: intron variant
orthologous variants: 85735811-C-T

46287184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: intron variant
orthologous variants: 85735815-T-C

http://identifiers.org/hco/22/GRCh38#46287192-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85735823-C-A

46287192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: intron variant
orthologous variants: 85735823-C-T

46287204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: intron variant
orthologous variants: 85735835-T-C

46287205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: intron variant
orthologous variants: 85735836-G-A

46287205-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: intron variant
orthologous variants: 85735836-G-T

46287263-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: intron variant
orthologous variants: 85735887-T-A

46287263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: intron variant
orthologous variants: 85735887-T-C

46287396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: intron variant
orthologous variants: 85735990-C-T

46287438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: intron variant
orthologous variants: 85736016-C-T

46287663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: intron variant
orthologous variants: 85736214-C-T

46288160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: intron variant
orthologous variants: 85736776-G-A

46288178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: intron variant
orthologous variants: 85736791-A-G

http://identifiers.org/hco/22/GRCh38#46288198-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85736827-A-C

46288275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: intron variant
orthologous variants: 85736886-G-A

46288275-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: intron variant
orthologous variants: 85736886-G-T

46288278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: intron_variant, undefined
orthologous variants: 85736888-G-A

46288278-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: intron_variant, undefined
orthologous variants: 85736888-G-T

http://identifiers.org/hco/22/GRCh38#46288292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#85736902-C-A

46288292-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: intron_variant, undefined
orthologous variants: 85736902-C-G

46288293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: intron_variant, undefined
orthologous variants: 85736903-C-T

http://identifiers.org/hco/22/GRCh38#46288318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#85736920-C-A

46288320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: intron_variant, undefined
orthologous variants: 85736922-G-A

46288339-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: intron_variant, undefined
orthologous variants: 85736941-G-T

46288343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: intron_variant, undefined
orthologous variants: 85736945-A-G

http://identifiers.org/hco/22/GRCh38#46288348-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#85736949-C-A

46288348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: intron_variant, undefined
orthologous variants: 85736949-C-T

46288349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: intron_variant, undefined
orthologous variants: 85736950-G-A

46288349-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: intron_variant, undefined
orthologous variants: 85736950-G-C

46288349-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: intron_variant, undefined
orthologous variants: 85736950-G-T

46288351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: intron_variant, undefined
orthologous variants: 85736952-G-A

46288351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: intron_variant, undefined
orthologous variants: 85736952-G-T

46288366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: intron_variant, undefined
orthologous variants: 85736967-A-G

http://identifiers.org/hco/22/GRCh38#46288389-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#85736988-C-A

46288396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: intron_variant, undefined
orthologous variants: 85736995-C-T

46288397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: intron_variant, undefined
orthologous variants: 85736996-C-T

http://identifiers.org/hco/22/GRCh38#46288522-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#85737120-C-A

46288522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, missense_variant, undefined
orthologous variants: 85737120-C-T

46288526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, synonymous_variant, undefined
orthologous variants: 85737124-C-T

46288639-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85737233-T-G

46288698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85737297-G-A

46288698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85737297-G-T

http://identifiers.org/hco/22/GRCh38#46288726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#85737328-C-A

46288754-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85737357-C-G

46288754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 85737357-C-T

http://identifiers.org/hco/22/GRCh38#46288996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85737484-C-A

46289080-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85737556-G-T

http://identifiers.org/hco/22/GRCh38#46289276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85737688-C-A

http://identifiers.org/hco/22/GRCh38#46289322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85737731-C-A

46289322-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85737731-C-G

46289322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85737731-C-T

46289323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85737732-G-A

46289323-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85737732-G-T

46289483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 85737867-C-T

46289599-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85737986-G-C

46289599-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85737986-G-T

46289601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85737988-G-A

46289601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85737988-G-T

46289606-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85737993-G-T

46289643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85738016-T-C

http://identifiers.org/hco/22/GRCh38#46289678-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85738063-C-A

http://identifiers.org/hco/22/GRCh38#46289693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85738078-C-A

46289693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85738078-C-T

46289695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85738080-T-C

46289773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85738134-C-T

http://identifiers.org/hco/22/GRCh38#46289795-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85738146-A-C

46289855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 85738206-C-T

46289858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 85738209-G-A

46289882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 85738233-C-T

http://identifiers.org/hco/22/GRCh38#46289921-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85738278-A-C

46289968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85738316-T-C

http://identifiers.org/hco/22/GRCh38#46289984-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85738325-C-A

46289984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85738325-C-T

46289997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85738337-G-T

http://identifiers.org/hco/22/GRCh38#46290046-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85738387-C-A

46290046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85738387-C-T

46290069-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85738410-T-G

46290080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85738420-A-G

46291568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85740163-G-A

46292739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85740622-C-T

46292767-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 85740650-G-T

http://identifiers.org/hco/22/GRCh38#46292909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85740788-C-A

46292909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 85740788-C-T

46292935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: 3 prime UTR variant
orthologous variants: 85740811-G-A

46292935-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: 3 prime UTR variant
orthologous variants: 85740811-G-T

46292961-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: 3 prime UTR variant
orthologous variants: 85740842-G-T

http://identifiers.org/hco/22/GRCh38#46293134-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85741023-C-A

http://identifiers.org/hco/22/GRCh38#46293261-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85741123-C-A

46293261-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: 3 prime UTR variant
orthologous variants: 85741123-C-G

46293261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: 3 prime UTR variant
orthologous variants: 85741123-C-T

46293262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: 3 prime UTR variant
orthologous variants: 85741124-A-G

46293262-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: 3 prime UTR variant
orthologous variants: 85741124-A-T

http://identifiers.org/hco/22/GRCh38#46293267-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85741130-C-A

46293267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: 3 prime UTR variant
orthologous variants: 85741130-C-T

46293268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: 3 prime UTR variant
orthologous variants: 85741131-T-C

46293269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: 3 prime UTR variant
orthologous variants: 85741132-G-A

46293269-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: 3 prime UTR variant
orthologous variants: 85741132-G-T

http://identifiers.org/hco/22/GRCh38#46293273-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85741136-C-A

46293273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: 3 prime UTR variant
orthologous variants: 85741136-C-T

46293275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: 3 prime UTR variant
orthologous variants: 85741138-G-A

46293275-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: 3 prime UTR variant
orthologous variants: 85741138-G-C

46293275-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: 3 prime UTR variant
orthologous variants: 85741138-G-T

46293276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: 3 prime UTR variant
orthologous variants: 85741139-T-C

46293280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: 3 prime UTR variant
orthologous variants: 85741143-C-T

http://identifiers.org/hco/22/GRCh38#46293302-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85741164-A-C

46293302-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: 3 prime UTR variant
orthologous variants: 85741164-A-T

http://identifiers.org/hco/22/GRCh38#46293361-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85741209-C-A

46293361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: 3 prime UTR variant
orthologous variants: 85741209-C-T

http://identifiers.org/hco/22/GRCh38#46293431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85741294-C-A

46293431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: 3 prime UTR variant
orthologous variants: 85741294-C-T

http://identifiers.org/hco/22/GRCh38#46293472-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85741336-A-C

http://identifiers.org/hco/22/GRCh38#46293496-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85741360-C-A

46293496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: 3 prime UTR variant
orthologous variants: 85741360-C-T

46293666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: 3 prime UTR variant
orthologous variants: 85742072-G-A

46293724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: 3 prime UTR variant
orthologous variants: 85742127-G-T

46293745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: 3 prime UTR variant
orthologous variants: 85742128-T-C

46293842-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: 3 prime UTR variant
orthologous variants: 85742172-A-T

46293920-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: 3 prime UTR variant
orthologous variants: 85742225-G-T

http://identifiers.org/hco/22/GRCh38#46293976-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26082
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#85742299-C-A