http://identifiers.org/hco/1/GRCh38#115976543-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#101831503-C-A

115976543-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101831503-C-G

115976543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101831503-C-T

115976585-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101831473-T-A

115976585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101831473-T-C

115976620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101831440-G-A

115976620-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101831440-G-C

115976620-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101831440-G-T

http://identifiers.org/hco/1/GRCh38#115976722-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#101831338-C-A

115976722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 101831338-C-T

http://identifiers.org/hco/1/GRCh38#115976723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#101831337-C-A

115976723-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101831337-C-G

115976723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101831337-C-T

115976797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101831302-G-T

115976843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101831276-G-A

115976864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101831254-G-A

115976864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101831254-G-T

115977113-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101831114-T-G

115977117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101831110-A-G

115977749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101830530-T-C

115977768-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101830511-T-A

115977773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101830506-A-G

115977792-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101830488-C-G

115977792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101830488-C-T

115978191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101830200-A-G

115978269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101830131-G-A

115981195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101829674-G-A

115981288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101829596-A-G

115985783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101828500-C-T

115985815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101828468-C-T

115985962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101828332-A-G

115985963-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101828331-A-T

115986063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101828272-G-T

115986127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101828216-G-A

115986127-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101828216-G-C

115986190-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101828189-G-T

115986255-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101828131-A-T

115986372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101828073-C-T

115986428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101828026-G-A

115986454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101827999-G-A

115986746-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101827336-A-G

115986840-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101827241-G-T

115986841-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101827240-A-T

115987072-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101827104-G-C

115987104-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101827072-G-T

115987625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101826878-T-C

115988098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101826463-A-G

115988151-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101826398-G-C

115988288-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101826263-T-G

115988331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101826224-C-T

115988543-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101826055-G-C

115988543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101826055-G-T

115988609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101826041-C-T

115988950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101825948-C-T

115989210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101825736-A-G

115989364-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101825626-T-A

115989403-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101825583-G-T

115990114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101825299-T-C

115990120-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101825294-G-C

115990508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101824940-A-G

115991077-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101824183-T-G

115991125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101824130-A-G

115991233-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101824020-C-G

115991459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101823854-A-G

115991814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101823567-T-C

115991824-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101823557-G-T

115991920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101823466-A-G

http://identifiers.org/hco/1/GRCh38#115991945-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#101822912-C-A

115991945-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101822912-C-G

115992122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 101822740-G-A

115992122-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 101822740-G-T

115992158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 101822704-T-C

115992220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 101822642-A-G

116005497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101818511-A-G

116005606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101818407-A-G

116005723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101818364-G-A

116005758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101818330-G-A

116005802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101818299-A-G

116006080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101817977-G-A

116006084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101817973-C-T

http://identifiers.org/hco/1/GRCh38#116006095-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#101817964-A-C

116006125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101817934-A-G

116006220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101817750-G-A

http://identifiers.org/hco/1/GRCh38#116006227-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#101817743-A-C

116006247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101817718-A-G

116006266-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101817699-C-G

116006563-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101817455-T-A

http://identifiers.org/hco/1/GRCh38#116006564-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#101817454-C-A

116006564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101817454-C-T

116006594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101817425-G-A

116006650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101817373-G-A

116006655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101817368-C-T

116006670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101817353-C-T

116006937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101816644-C-T

116006992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101816596-C-T

116007026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101816560-G-A

116007417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 101816247-A-G

116007605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101816057-A-G

116008638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101814455-G-A

116009064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101814057-G-T

116009154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101813830-C-T

116009290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101813714-G-A

116009638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101813405-A-G

116009670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101813376-G-A

116009847-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101813123-C-G

116010149-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101812845-G-C

116010427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101812563-T-C

116010455-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101812535-G-C

116010480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101812510-T-C

116010748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101812268-G-A

116010879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101812144-C-T

116011024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101812009-A-G

116011084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101811949-G-A

116011644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101811348-A-G

116011709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101811284-A-G

116011774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101811193-G-A

116011852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101811103-A-G

116011865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101811090-A-G

116011906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101811053-A-G

http://identifiers.org/hco/1/GRCh38#116011924-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#101811035-C-A

116012191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101810762-T-C

116012287-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101810665-T-G

116012297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101810655-C-T

116012477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101810606-T-C

116012582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101810521-G-A

116013438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101809912-A-G

116013465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101809884-A-G

http://identifiers.org/hco/1/GRCh38#116013617-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#101809736-A-C

116013646-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101809705-T-A

116013673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101809662-A-G

116013673-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101809662-A-T

116013750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101809589-A-G

116013753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101809586-T-C

http://identifiers.org/hco/1/GRCh38#116013937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#101809421-C-A

116014028-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101809264-C-G

116014496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101808838-G-A

116014587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101808223-A-G

http://identifiers.org/hco/1/GRCh38#116014607-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#101808203-A-C

116014676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101808133-G-A

116014954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101807874-G-A

http://identifiers.org/hco/1/GRCh38#116014958-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#101807870-A-C

116015159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101807693-C-T

116015289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101807579-T-C

116015350-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101807528-T-A

116015356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101807522-G-A

116015356-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101807522-G-C

116015356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101807522-G-T

116015878-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101807064-T-G

116017666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101806705-G-A

116017719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101806651-T-C

116017732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101806638-T-C

116017759-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101806611-T-A

116017795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101806592-A-G

116017830-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101806558-T-G

116017862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101806525-T-C

116018047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101806356-G-A

116018257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101806182-A-G

116019141-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101805825-A-T

116019432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101805545-G-A

116019432-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101805545-G-C

116019432-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101805545-G-T

116019459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101805520-A-G

http://identifiers.org/hco/1/GRCh38#116019463-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#101805516-C-A

116019473-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101805506-G-T

116019570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101805403-A-G

116019570-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101805403-A-T

http://identifiers.org/hco/1/GRCh38#116019576-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#101805389-C-A

116019576-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 101805389-C-G

116019576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 101805389-C-T

116019589-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 101805376-T-G

116019594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 101805371-G-A

116019596-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 101805369-C-G

116019599-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 101805366-C-G

116019619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 101805346-C-T

116019629-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 101805336-T-G

116019762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101805203-T-C

116019762-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101805203-T-G

116019826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101805137-A-G

116019851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101805112-G-A

116019851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101805112-G-T

116019852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101805111-G-A

116019852-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101805111-G-T

http://identifiers.org/hco/1/GRCh38#116019853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#101805110-C-A

116020042-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101804923-T-G

116020226-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101804741-T-A

116020226-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101804741-T-G

http://identifiers.org/hco/1/GRCh38#116020665-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#101804645-C-A

116020665-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101804645-C-G

116020692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101804618-G-A

116020692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101804618-G-T

116020750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 101804559-G-T

116020865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 101804444-C-T

116024020-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101794748-T-A

116024174-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101794573-G-T

116024502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101794234-A-G

116025166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101792643-C-T

116025265-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101792575-C-G

116025558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101792259-A-G

116025612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101792046-G-A

116025693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101791954-T-C

116026228-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101791478-A-G

116026420-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101791357-T-A

116026420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101791357-T-C

116026655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101791133-A-G

116026739-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101791049-G-C

116026776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101791018-A-G

116026776-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101791018-A-T

116026844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101790950-G-A

116026913-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 101790883-T-A

116026922-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 101790874-G-T

116027281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101790516-C-T

116027309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101790471-T-C

116027353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101790428-G-A

116027446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101790335-T-C

116028313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101789814-A-G

116028322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101789805-A-G

116028349-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101789778-G-C

116028349-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101789778-G-T

116028495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101789639-A-G

116028508-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101789626-A-T

116028563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101789584-G-T

116029949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101789269-T-C

116030158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101789080-A-G

116030242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101789002-A-G

116030605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101788377-A-G

http://identifiers.org/hco/1/GRCh38#116030690-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#101788289-C-A

http://identifiers.org/hco/1/GRCh38#116030725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#101788254-C-A

116030838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101788140-T-C

116030839-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101788139-C-G

116030882-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101788095-A-T

116030883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101788094-A-G

116030883-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101788094-A-T

116030944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101788017-A-G

116031175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101787702-G-A

116031179-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101787698-A-T

116031183-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101787694-C-G

116031252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101787651-T-C

http://identifiers.org/hco/1/GRCh38#116031290-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#101787613-C-A

116031290-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101787613-C-G

116031418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 101787486-G-A

116031418-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 101787486-G-T

http://identifiers.org/hco/1/GRCh38#116031529-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#101787375-C-A

116031529-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 101787375-C-G

116031529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 101787375-C-T

116031547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 101787357-C-T

116031600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101787307-G-A

116031675-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101787228-T-G

116032135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101787047-C-T

116032729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101786807-G-T

http://identifiers.org/hco/1/GRCh38#116032747-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#101786790-A-C

116032747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101786790-A-G

116032782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101786755-A-G

116032819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101786724-G-A

116032819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101786724-G-T

116032825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101786718-A-G

116032833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101786710-T-C

116032845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101786698-A-G

http://identifiers.org/hco/1/GRCh38#116032847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#101786696-C-A

116033991-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101786444-G-C

116034360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101786105-G-A

116034479-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101785976-T-G

116034754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101785736-T-C

116034763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101785727-G-A

116034954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101785537-A-G

116035049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101785447-G-T

116035092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101785413-G-T

http://identifiers.org/hco/1/GRCh38#116035096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#101785409-C-A

116035165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101785345-G-A

116035165-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101785345-G-C

116035369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101785145-G-A

116035369-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101785145-G-T

http://identifiers.org/hco/1/GRCh38#116035397-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#101785119-A-C

http://identifiers.org/hco/1/GRCh38#116035398-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#101785118-C-A

116035401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101785115-G-A

116035445-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101785074-G-C

116035445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101785074-G-T

116035779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101784820-T-C

116035789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101784810-A-G

116036342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101783951-C-T

116036525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101783755-C-T

116036534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101783746-G-A

116036770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101783556-T-C

116036816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101783508-G-A

http://identifiers.org/hco/1/GRCh38#116037473-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#101782876-C-A

116037473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 101782876-C-T

116038316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 101781497-G-A

116038575-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron variant
orthologous variants: 101781227-G-T

116038678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron variant
orthologous variants: 101781193-C-T

116038756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron variant
orthologous variants: 101781124-A-G

116038892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron variant
orthologous variants: 101781001-C-T

116039646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 101780604-T-C

116039708-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 101780539-A-T

116040222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 101780002-A-G

116041056-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 101779540-G-T

http://identifiers.org/hco/1/GRCh38#116041185-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#101779424-C-A

116041185-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 101779424-C-G

116041185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 101779424-C-T

116041247-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 101779364-T-G

116041438-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 101779187-T-G

116041509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 101779131-C-T

116041705-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 101778942-G-T

http://identifiers.org/hco/1/GRCh38#116041708-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#101778939-A-C

116060003-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron variant
orthologous variants: 101774713-G-T

116060103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron variant
orthologous variants: 101774619-C-T

116060166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron variant
orthologous variants: 101774564-A-G

116060268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron variant
orthologous variants: 101774489-A-G

116060393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron variant
orthologous variants: 101774384-A-G

116060480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron variant
orthologous variants: 101774297-C-T

116060515-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron variant
orthologous variants: 101774266-T-A

116060515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron variant
orthologous variants: 101774266-T-C

116060787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron variant
orthologous variants: 101773433-T-C

116061311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron variant
orthologous variants: 101772982-G-A

116061311-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron variant
orthologous variants: 101772982-G-T

116062701-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron variant
orthologous variants: 101771983-T-A

116062701-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron variant
orthologous variants: 101771983-T-C

116062743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron variant
orthologous variants: 101771941-T-C

116062776-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, missense_variant
orthologous variants: 101771910-G-C

116062784-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 101771902-G-T

116062801-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron_variant, missense_variant
orthologous variants: 101771885-C-G

116062897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron variant
orthologous variants: 101771789-C-T

http://identifiers.org/hco/1/GRCh38#116062943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#101771741-C-A

116063176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron variant
orthologous variants: 101771631-G-A

116063289-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron variant
orthologous variants: 101771576-G-T

116063456-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron variant
orthologous variants: 101771488-G-T

http://identifiers.org/hco/1/GRCh38#116063577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#101771378-C-A

116063627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron variant
orthologous variants: 101771332-A-G

116063837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron variant
orthologous variants: 101771169-C-T

116063856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron variant
orthologous variants: 101771166-A-G

116063909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron variant
orthologous variants: 101771117-C-T

http://identifiers.org/hco/1/GRCh38#116063954-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#101771084-A-C

116064253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron variant
orthologous variants: 101770462-G-A

116064343-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron variant
orthologous variants: 101770406-A-T

http://identifiers.org/hco/1/GRCh38#116064392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#101770353-C-A

116064533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron variant
orthologous variants: 101770194-T-C

116064533-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron variant
orthologous variants: 101770194-T-G

116064552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron variant
orthologous variants: 101770178-T-C

116064581-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron variant
orthologous variants: 101770149-G-C

116064608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron variant
orthologous variants: 101770123-T-C

116064797-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron variant
orthologous variants: 101769944-T-A

116064798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron variant
orthologous variants: 101769943-A-G

116064833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron variant
orthologous variants: 101769922-G-A

116064854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron variant
orthologous variants: 101769906-A-G

116064854-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron variant
orthologous variants: 101769906-A-T

116064884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron variant
orthologous variants: 101769876-G-A

116064895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron variant
orthologous variants: 101769865-T-C

116064972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron variant
orthologous variants: 101769800-C-T

http://identifiers.org/hco/1/GRCh38#116065908-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#101768887-A-C

116065913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron variant
orthologous variants: 101768882-A-G

116066074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron variant
orthologous variants: 101768748-T-C

116066365-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron variant
orthologous variants: 101768457-C-G

116066498-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron variant
orthologous variants: 101768325-A-T

http://identifiers.org/hco/1/GRCh38#116066501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#101768322-C-A

116066501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron variant
orthologous variants: 101768322-C-T

http://identifiers.org/hco/1/GRCh38#116066511-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#101768312-C-A

116066511-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron variant
orthologous variants: 101768312-C-G

116066511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron variant
orthologous variants: 101768312-C-T

116066699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 101768124-C-T

http://identifiers.org/hco/1/GRCh38#116066977-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#101767870-C-A

116066977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: intron variant
orthologous variants: 101767870-C-T

116067017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: splice acceptor variant
orthologous variants: 101767835-A-G

116067020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 101767832-G-A

116067020-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 101767832-G-T

116067232-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3 prime UTR variant
orthologous variants: 101767683-T-G

116067267-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3 prime UTR variant
orthologous variants: 101767644-T-A

116067267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3 prime UTR variant
orthologous variants: 101767644-T-C

116067270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3 prime UTR variant
orthologous variants: 101767641-G-T

116067300-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3 prime UTR variant
orthologous variants: 101767612-T-A

116067300-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3 prime UTR variant
orthologous variants: 101767612-T-G

116067458-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3 prime UTR variant
orthologous variants: 101767482-G-C

116067467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 101767473-G-A

116067477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 101767463-T-C

116067580-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3 prime UTR variant
orthologous variants: 101767362-G-T

116067606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 101767353-G-A

116067606-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 101767353-G-C

http://identifiers.org/hco/1/GRCh38#116067670-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#101767324-A-C

116067741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3 prime UTR variant
orthologous variants: 101767271-A-G

116067745-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3 prime UTR variant
orthologous variants: 101767267-G-C

116067745-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3 prime UTR variant
orthologous variants: 101767267-G-T

http://identifiers.org/hco/1/GRCh38#116067770-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#101767242-C-A

116067770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3 prime UTR variant
orthologous variants: 101767242-C-T

116067841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3 prime UTR variant
orthologous variants: 101767178-T-C

116067863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3 prime UTR variant
orthologous variants: 101767158-T-C

116067875-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3 prime UTR variant
orthologous variants: 101767146-G-T

http://identifiers.org/hco/1/GRCh38#116067918-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#101767092-A-C

116067918-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3 prime UTR variant
orthologous variants: 101767092-A-T

http://identifiers.org/hco/1/GRCh38#116067923-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#101767087-A-C

116067923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3 prime UTR variant
orthologous variants: 101767087-A-G

116067959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3 prime UTR variant
orthologous variants: 101767049-A-G

116068077-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3 prime UTR variant
orthologous variants: 101766971-C-G

http://identifiers.org/hco/1/GRCh38#116068110-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#101766935-C-A

116068110-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3 prime UTR variant
orthologous variants: 101766935-C-G

116068110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3 prime UTR variant
orthologous variants: 101766935-C-T

http://identifiers.org/hco/1/GRCh38#116068299-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#101766773-C-A

116068299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3 prime UTR variant
orthologous variants: 101766773-C-T

http://identifiers.org/hco/1/GRCh38#116068449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#101766631-C-A

116068462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3 prime UTR variant
orthologous variants: 101766620-A-G

116068509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3 prime UTR variant
orthologous variants: 101766575-T-C

http://identifiers.org/hco/1/GRCh38#116068519-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#101766565-C-A

116068530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3 prime UTR variant
orthologous variants: 101766555-G-T

116068556-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3 prime UTR variant
orthologous variants: 101766533-G-C

116068637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3 prime UTR variant
orthologous variants: 101766486-A-G

http://identifiers.org/hco/1/GRCh38#116068701-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#101766422-C-A

116068819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3 prime UTR variant
orthologous variants: 101766308-G-T

116068966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3 prime UTR variant
orthologous variants: 101765664-A-G

116068984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3 prime UTR variant
orthologous variants: 101765649-C-T

116068990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3 prime UTR variant
orthologous variants: 101765643-C-T

116069023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3 prime UTR variant
orthologous variants: 101765612-T-C

116069061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3 prime UTR variant
orthologous variants: 101765597-T-C

116069062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3 prime UTR variant
orthologous variants: 101765596-A-G

http://identifiers.org/hco/1/GRCh38#116069100-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#101765556-C-A

116069150-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3 prime UTR variant
orthologous variants: 101765520-G-T

116069195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3 prime UTR variant
orthologous variants: 101765483-A-G

116069512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3 prime UTR variant
orthologous variants: 101765172-A-G

http://identifiers.org/hco/1/GRCh38#116069645-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#101765001-C-A

116069681-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3 prime UTR variant
orthologous variants: 101764968-G-T

116069801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3 prime UTR variant
orthologous variants: 101764866-A-G

http://identifiers.org/hco/1/GRCh38#116069862-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#101764828-C-A

116069945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3 prime UTR variant
orthologous variants: 101764744-A-G

116069946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3 prime UTR variant
orthologous variants: 101764743-T-C

116070018-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20301
most severe consequence: 3 prime UTR variant
orthologous variants: 101764322-G-T