157081729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 65770747-T-C

http://identifiers.org/hco/3/GRCh38#157081782-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#65770799-C-A

157081782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 65770799-C-T

157081784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 65770801-G-A

157081784-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 65770801-G-T

157081884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: non coding transcript exon variant
orthologous variants: 65770910-G-A

157081884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: non coding transcript exon variant
orthologous variants: 65770910-G-T

157081932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 65770957-G-A

157081932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 65770957-G-T

http://identifiers.org/hco/3/GRCh38#157081995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#65771014-C-A

157081998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 65771017-T-C

157082024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: non coding transcript exon variant
orthologous variants: 65771047-G-A

http://identifiers.org/hco/3/GRCh38#157082054-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#65771081-A-C

http://identifiers.org/hco/3/GRCh38#157082094-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#65771129-C-A

157082094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: non coding transcript exon variant
orthologous variants: 65771129-C-T

157082139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 65771173-T-C

157082139-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 65771173-T-G

157082240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: non coding transcript exon variant
orthologous variants: 65771268-C-T

157082382-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: non coding transcript exon variant
orthologous variants: 65771402-C-G

157082460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: non coding transcript exon variant
orthologous variants: 65771476-T-C

157082513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: non coding transcript exon variant
orthologous variants: 65771525-T-C

157082645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65771658-G-A

157082649-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65771662-G-C

http://identifiers.org/hco/3/GRCh38#157082783-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#65771788-C-A

157082800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 65771805-A-G

157082805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 65771810-T-C

157082921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 65771929-A-G

http://identifiers.org/hco/3/GRCh38#157082949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#65771956-C-A

157082949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65771956-C-T

157082977-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65771976-G-T

http://identifiers.org/hco/3/GRCh38#157083025-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#65772016-C-A

157083194-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65772180-T-A

http://identifiers.org/hco/3/GRCh38#157083210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#65772194-C-A

157083210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65772194-C-T

157083213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65772197-G-A

157083213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65772197-G-T

157083228-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65772205-G-T

157083284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65772255-G-A

157083284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65772255-G-T

http://identifiers.org/hco/3/GRCh38#157083309-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#65772280-C-A

157083493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65772465-C-T

http://identifiers.org/hco/3/GRCh38#157083674-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#65772585-C-A

157083848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65772746-G-A

157084276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65774440-G-A

157084276-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65774440-G-C

157084569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65774710-G-A

157084646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65774779-A-G

157084937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65775031-C-T

157085358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65775378-G-A

157085707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65775769-G-A

157085769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65775826-A-G

157085841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65775888-C-T

157085977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65776001-T-C

http://identifiers.org/hco/3/GRCh38#157086348-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#65776286-C-A

157086445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65776382-G-A

157086457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65776394-C-T

157086468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65776404-G-A

157086602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65776537-G-A

157087065-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65776989-G-T

157087675-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65777553-T-A

157087675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65777553-T-C

157087702-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65777565-T-G

157087858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 65777690-G-A

157087858-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 65777690-G-T

157087934-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65777763-G-C

http://identifiers.org/hco/3/GRCh38#157088189-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#65777987-C-A

157088406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65778124-G-A

157088494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65778206-C-T

157088496-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65778207-G-T

157088643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65778353-A-G

157088731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65778431-A-G

157088772-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65778466-C-G

157088772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65778466-C-T

157088923-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65778623-T-A

157088923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65778623-T-C

157089294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65778971-C-T

http://identifiers.org/hco/3/GRCh38#157089384-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#65779057-C-A

157089533-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65779184-T-G

157089698-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65779335-T-G

http://identifiers.org/hco/3/GRCh38#157089740-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#65779359-C-A

157090091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 65779595-G-A

157090358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65779826-T-C

157090407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65779875-T-C

157090476-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65779935-T-A

157090478-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65779937-T-A

157090591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65780038-A-G

157090691-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65780331-T-C

http://identifiers.org/hco/3/GRCh38#157091123-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#65780788-A-C

157091191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65780867-C-T

157091242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65780909-G-A

157092251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65781060-G-A

157092251-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65781060-G-C

157092263-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65781072-A-T

157092365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65781173-A-G

157092457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65781262-G-A

http://identifiers.org/hco/3/GRCh38#157092658-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#65781471-A-C

157092773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65781555-C-T

157092786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65781568-T-C

157094261-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65785044-G-C

157094412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65785191-A-G

157094608-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65785373-G-C

157094682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65785449-G-A

157094703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65785470-G-A

157094779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65785540-A-G

157095159-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65785917-G-T

157095596-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65786487-G-C

157095725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65786598-G-A

157095794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65786663-T-C

157095796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65786665-G-T

157096256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65786758-G-A

157096356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65786849-G-A

http://identifiers.org/hco/3/GRCh38#157096369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#65786862-C-A

157096438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65786930-G-A

157096555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65787040-C-T

157096569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65787054-C-T

157098668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65790890-C-T

157099029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65791652-G-A

157099200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65791816-T-C

157099397-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65791993-G-T

157099403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65791999-G-A

http://identifiers.org/hco/3/GRCh38#157099471-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#65792066-C-A

157099471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65792066-C-T

157099523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65792116-C-T

http://identifiers.org/hco/3/GRCh38#157099572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#65792166-C-A

157099592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65792186-G-A

157099592-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65792186-G-T

157099601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65792195-G-A

157099601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65792195-G-T

http://identifiers.org/hco/3/GRCh38#157099669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#65792265-C-A

157099669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65792265-C-T

http://identifiers.org/hco/3/GRCh38#157099731-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#65792327-C-A

http://identifiers.org/hco/3/GRCh38#157099795-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#65792392-C-A

157099795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65792392-C-T

157103571-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65796005-G-T

157103615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65796043-T-C

157103652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65796087-C-T

157103771-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65796206-G-T

157103784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65796218-C-T

157104559-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65796968-C-G

157104559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65796968-C-T

http://identifiers.org/hco/3/GRCh38#157104589-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#65796998-C-A

http://identifiers.org/hco/3/GRCh38#157104636-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#65797044-A-C

157104780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65797191-C-T

157104787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65797198-G-T

http://identifiers.org/hco/3/GRCh38#157104892-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#65797364-A-C

157104986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65797474-C-T

157105410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65798424-C-T

157105517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65798529-C-T

157105679-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65798689-G-C

157105933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65798940-G-A

157106002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65799008-C-T

157106004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65799010-G-A

157106062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65799060-C-T

157106366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65801275-C-T

157106738-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65801569-T-G

157106760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 65801591-G-A

157107061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65802335-G-A

157107129-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65802401-C-G

157107129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65802401-C-T

157107245-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65802489-T-A

157107246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65802490-G-A

157107433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65802674-C-T

157107581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65803041-G-A

157107710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65803183-G-A

157107755-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65803227-C-G

157108019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65803476-C-T

http://identifiers.org/hco/3/GRCh38#157108676-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#65804036-A-C

157108676-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65804036-A-T

157108687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65804047-A-G

157108762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65804121-G-A

157109118-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65804471-A-G

http://identifiers.org/hco/3/GRCh38#157109121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#65804474-C-A

157109121-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65804474-C-G

157109790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65805141-G-A

157109810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65805183-C-T

157110047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65805415-G-A

157110146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65805485-A-G

157110661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65805848-T-C

157110716-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65805899-G-T

http://identifiers.org/hco/3/GRCh38#157111175-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#65806336-A-C

157111670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65806982-G-A

157111670-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65806982-G-T

157111949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65807228-A-G

157112039-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65807336-G-C

157112080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65807377-T-C

157114794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65811799-A-G

157115108-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65812035-G-C

157115228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65812148-G-A

157115585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65812621-C-T

http://identifiers.org/hco/3/GRCh38#157116221-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#65813354-A-C

157116280-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65813410-T-A

157116537-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65813651-G-C

157116566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65813680-G-A

157116675-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65813790-T-A

157116711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65813826-T-C

157116857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65813975-G-A

157117021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65814110-T-C

157117259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65814578-G-T

157117482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65814869-A-G

157117515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65814905-C-T

157117520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65814910-G-A

157117524-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65814914-C-G

157117524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65814914-C-T

157117662-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65815051-G-T

157117713-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65815091-C-G

157117722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65815100-A-G

157117733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65815111-A-G

157117788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65815165-A-G

157117910-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65815441-A-T

157118958-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65818146-A-T

157119064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65818269-T-C

http://identifiers.org/hco/3/GRCh38#157119207-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#65818499-A-C

157119207-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65818499-A-T

157119307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65818614-T-C

157119307-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65818614-T-G

157120727-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65826871-A-T

157121130-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65827921-G-T

157121247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65828284-G-A

http://identifiers.org/hco/3/GRCh38#157121257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#65828294-C-A

157121340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65828373-G-A

157121785-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65829619-A-T

157121800-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65829628-T-A

http://identifiers.org/hco/3/GRCh38#157122203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#65829999-C-A

http://identifiers.org/hco/3/GRCh38#157122309-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#65830103-C-A

157122333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65830124-T-C

157122366-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65830156-G-C

157122657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65830385-C-T

157122690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65830429-T-C

157122798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65830533-G-A

157122823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65830558-A-G

157122864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65830598-T-C

157122923-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65830634-T-A

http://identifiers.org/hco/3/GRCh38#157122943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#65830661-C-A

157122943-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65830661-C-G

157122951-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65830669-G-T

157123018-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65830732-G-T

http://identifiers.org/hco/3/GRCh38#157123041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#65830802-C-A

157123041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65830802-C-T

157123068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65830829-C-T

157123451-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65831597-T-G

157123534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65831677-A-G

157123534-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65831677-A-T

157123573-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65831716-T-G

157123758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65831885-A-G

157123830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65831955-G-A

157124447-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65833585-T-G

157124567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65833477-A-G

157124762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65833275-A-G

157125077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65832789-A-G

157128242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27948
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65834431-G-A