69466761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 5 prime UTR variant
orthologous variants: 12762720-T-C

69466941-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 12762899-T-G

69467011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12763124-G-A

69467011-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12763124-G-T

69467076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12763189-G-A

69467076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12763189-G-T

69467181-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12763293-G-C

http://identifiers.org/hco/8/GRCh38#69467216-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12763323-C-A

69467476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12763557-T-C

69468416-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12764453-T-A

69468417-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12764454-A-T

69468545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12764564-G-A

69468551-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12764570-G-C

69468872-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12764899-T-A

69468872-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12764899-T-G

http://identifiers.org/hco/8/GRCh38#69469125-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12765162-C-A

69469165-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12765202-A-T

http://identifiers.org/hco/8/GRCh38#69469251-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12765289-C-A

http://identifiers.org/hco/8/GRCh38#69469322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12765355-C-A

69469322-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12765355-C-G

69469322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12765355-C-T

69469440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12765470-T-C

69469448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12765478-T-C

69469455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12765485-A-G

http://identifiers.org/hco/8/GRCh38#69469476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12765503-C-A

69469476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12765503-C-T

69469622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12765638-C-T

69469703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12765713-A-G

69470177-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12765873-C-G

69470546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12766245-A-G

69470546-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12766245-A-T

http://identifiers.org/hco/8/GRCh38#69470816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12766471-C-A

69470816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12766471-C-T

69470817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12766472-C-T

69471212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12766873-T-C

69471544-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12767177-T-A

69471599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12767234-G-A

69471812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12767422-T-C

69472021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12767543-G-A

69472064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12767568-T-C

69472372-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12768021-T-A

69472419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12768063-G-A

69472536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12768187-C-T

69472553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12768209-T-C

69473046-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12768622-C-G

69473299-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12768804-G-C

69473306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12768811-C-T

69473332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 12768837-T-C

http://identifiers.org/hco/8/GRCh38#69473386-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12768863-C-A

69473411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12768888-A-G

http://identifiers.org/hco/8/GRCh38#69473433-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12768910-A-C

69473444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12768915-G-A

69473444-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12768915-G-T

69473920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12769797-A-G

69474186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12770044-C-T

69474299-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12770146-T-A

69474564-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12770413-T-A

69476094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12771336-G-A

69476170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12771412-A-G

69476631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12772272-A-G

69476648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12772289-A-G

69476701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12772342-C-T

69476761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12772402-G-A

69477069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12772830-A-G

69477087-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12772848-T-C

http://identifiers.org/hco/8/GRCh38#69477306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12773117-C-A

69477306-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12773117-C-G

69477525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12773597-G-A

69477543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12773615-C-T

69478314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12774179-C-T

69478594-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12774413-G-C

69478625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12774464-C-T

http://identifiers.org/hco/8/GRCh38#69478862-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12774685-C-A

69478939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12774755-T-C

69479229-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12775039-T-G

http://identifiers.org/hco/8/GRCh38#69479304-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12775114-C-A

69479628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12775431-A-G

69479628-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12775431-A-T

69479722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12775476-C-T

69479924-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12776170-C-G

69479924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12776170-C-T

69480301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12776861-G-A

69480584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12777210-T-C

69481286-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12777811-T-G

http://identifiers.org/hco/8/GRCh38#69482176-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12778258-C-A

69482307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12778391-T-C

http://identifiers.org/hco/8/GRCh38#69482326-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12778410-C-A

69484142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12780582-T-C

69484422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12780875-T-C

69484485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12780938-T-C

69484485-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12780938-T-G

69484493-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12780946-C-G

69484538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12780995-C-T

69484841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12781359-T-C

http://identifiers.org/hco/8/GRCh38#69485211-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12781672-A-C

69485216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12781677-A-G

69485638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12782035-C-T

69485662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12782057-G-A

69485779-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12782172-G-T

69485785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12782178-A-G

69486515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12783100-T-C

69486559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12783144-G-T

http://identifiers.org/hco/8/GRCh38#69486575-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12783160-A-C

69486575-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12783160-A-T

69486577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12783218-G-A

69486597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12783238-G-A

69486597-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12783238-G-C

69486603-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12783244-G-C

69486679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12783303-C-T

69486795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12783398-C-T

69487147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12783685-G-T

69487522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12784061-C-T

http://identifiers.org/hco/8/GRCh38#69487980-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12785064-A-C

69488157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12785231-T-C

69488875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12785886-A-G

69491892-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12787266-G-C

69491984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12787348-G-A

69492067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12787424-G-A

69492269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12788165-G-A

69492398-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12788274-G-C

69492622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12788497-A-G

69492668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12788550-T-C

69492668-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12788550-T-G

69492725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12788607-T-C

69492876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12788755-G-A

http://identifiers.org/hco/8/GRCh38#69492891-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12788769-C-A

69492891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12788769-C-T

69492928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12788806-G-A

http://identifiers.org/hco/8/GRCh38#69493025-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12788907-C-A

http://identifiers.org/hco/8/GRCh38#69493056-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12788939-A-C

69493056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12788939-A-G

69493076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12788959-T-C

http://identifiers.org/hco/8/GRCh38#69493079-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12788962-C-A

69493079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12788962-C-T

69493157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12789033-A-G

69493272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12789138-G-A

69493563-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12789373-T-A

69493699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12789502-C-T

69493804-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12789608-A-T

69493807-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12789611-C-G

69493807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12789611-C-T

69494011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12789797-A-G

69494323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12790132-A-G

69494329-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12790138-T-G

http://identifiers.org/hco/8/GRCh38#69494378-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12790170-A-C

69494378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12790170-A-G

http://identifiers.org/hco/8/GRCh38#69494637-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12790508-C-A

69495546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12793079-A-G

http://identifiers.org/hco/8/GRCh38#69495762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12793267-C-A

69495762-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 12793267-C-G

http://identifiers.org/hco/8/GRCh38#69495775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12793277-C-A

69495783-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12793286-G-C

69496011-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12793674-G-T

69496024-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12793687-G-T

69496328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12793978-C-T

69496753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12795322-C-T

69496897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12795445-C-T

69496969-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12795519-T-A

69497019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12795568-G-A

69497562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12795794-T-C

69497756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12795959-C-T

http://identifiers.org/hco/8/GRCh38#69497782-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12795984-A-C

69497790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12795992-A-G

69497888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12796057-A-G

69497956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12796115-A-G

69498005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12796165-A-G

69498137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12796260-A-G

69498155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12796277-G-A

69498182-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12796301-T-A

69498685-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12796973-C-G

69498742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12797010-A-G

69500395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12797866-A-G

69500472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12797934-G-A

69500472-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12797934-G-T

69501009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12798069-A-G

69501060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12798120-A-G

69501072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12798132-C-T

69501432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12798472-T-C

69501860-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12798804-C-G

69501898-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 12798842-C-G

http://identifiers.org/hco/8/GRCh38#69501920-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12798864-A-C

http://identifiers.org/hco/8/GRCh38#69502016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12798964-C-A

69502141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12799072-T-C

69502157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12799088-C-T

69502181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12799113-C-T

69502311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12799249-T-C

69502471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12799402-G-A

69503663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12800224-C-T

http://identifiers.org/hco/8/GRCh38#69503809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12800356-C-A

69503809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12800356-C-T

69504591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12800512-G-A

http://identifiers.org/hco/8/GRCh38#69504614-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12800531-A-C

69504639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12800558-T-C

69504679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12800597-T-C

69505206-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12801758-T-G

69505398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12801927-G-A

69505453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12801982-C-T

69505738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12803536-A-G

69505738-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12803536-A-T

http://identifiers.org/hco/8/GRCh38#69506150-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12803979-A-C

69506155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12803984-G-A

69506188-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12804016-T-A

69506349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12804147-C-T

69506371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12804170-C-T

69506687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12804574-A-G

69506886-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12804810-A-G

69506958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12804882-T-C

http://identifiers.org/hco/8/GRCh38#69507005-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12804930-A-C

69507067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12804996-G-A

69507076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12805005-C-T

69507153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12805079-A-G

69507197-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12805119-G-T

69507254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12805173-A-G

http://identifiers.org/hco/8/GRCh38#69507326-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12805245-C-A

69507326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12805245-C-T

69507672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12805527-G-A

69507678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12805533-T-C

69507688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12805543-A-G

69507790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12805649-G-A

69508526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12806232-C-T

69508715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12806429-A-G

69508738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12806448-T-C

69508881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12806604-G-A

69508949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12806645-T-C

69508949-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12806645-T-G

69508998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12806677-T-C

69509077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12806753-T-C

69509155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12806826-G-A

69509633-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12807278-A-G

69509683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12807339-A-G

69509698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12807353-G-A

69509716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12807370-G-A

69509847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12807490-C-T

69509977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12807622-C-T

http://identifiers.org/hco/8/GRCh38#69518210-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12812081-A-C

69519673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12813365-A-G

69520349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12814486-A-G

69520381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12814518-A-G

69520485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12814621-A-G

69520485-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12814621-A-T

69520496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12814630-G-A

69520537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12814663-A-G

69520617-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12814720-T-A

69520947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12815066-A-G

69520955-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12815074-C-G

69521150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12815273-A-G

69521210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12815336-T-C

69524720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12819252-G-A

69524787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12819293-A-G

69525206-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12819717-A-T

69525228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12819739-G-A

http://identifiers.org/hco/8/GRCh38#69525247-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12819758-C-A

69525544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12820062-T-C

69525724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12820538-A-G

69525739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12820553-T-C

69525886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12820691-G-A

69526140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12820923-G-A

69526160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12820940-T-C

69527044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12823201-G-A

69527069-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12823226-T-G

69527150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12823302-C-T

69527423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12823583-A-G

69527423-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12823583-A-T

69527611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12823729-G-A

69527628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12823746-T-C

69528577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12824838-T-C

69528595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12824855-T-C

69528667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12824984-A-G

69528861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12825141-A-G

69529067-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12825345-T-G

69529083-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12825361-T-G

69529234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12825525-T-C

69529368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12825663-A-G

69529571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12825875-A-G

69529685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12825994-A-G

69529837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12826141-T-C

69529883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12826174-T-C

69529913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12826204-G-A

69529919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12826210-G-A

http://identifiers.org/hco/8/GRCh38#69530059-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12826355-C-A

69530059-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12826355-C-G

69530144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12826440-G-A

69530271-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12826556-A-T

69531598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12827485-C-T

http://identifiers.org/hco/8/GRCh38#69531605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12827497-C-A

69531881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12827789-G-A

69531987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12827885-G-A

69531987-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12827885-G-T

69533978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12829928-A-G

69534235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12830165-G-A

69534304-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12830233-T-A

69534550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12830465-G-A

69534643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12830557-C-T

69534848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12830798-G-A

69535327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12831215-G-A

69535430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12831316-G-A

69535430-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12831316-G-T

http://identifiers.org/hco/8/GRCh38#69536659-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12832000-C-A

69536824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12832140-G-A

69536824-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12832140-G-T

http://identifiers.org/hco/8/GRCh38#69537275-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12832543-C-A

69537275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12832543-C-T

69537467-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12832703-G-T

69537489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12832716-G-T

69537511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12832735-A-G

http://identifiers.org/hco/8/GRCh38#69537536-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12832772-A-C

69537586-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12832816-G-T

69538454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12833610-C-T

69538524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12833680-C-T

http://identifiers.org/hco/8/GRCh38#69538586-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12833744-C-A

69539076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12833883-G-A

69539649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12834527-T-C

69539937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12834826-T-C

69541360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12835894-C-T

69541687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12836201-G-A

69542156-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12836791-A-T

69542173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12836808-A-G

69542173-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12836808-A-T

69542333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12836926-C-T

69542396-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12837003-T-A

69542396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12837003-T-C

69544183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12837942-T-C

69544971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12838555-G-A

69544982-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12838566-C-G

69545031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12838609-T-C

69545171-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12838737-T-A

69545181-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12838747-T-A

69546256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12839601-C-T

69546394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12839740-A-G

69546510-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12839856-T-A

69546586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12839949-A-G

69546633-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12839991-A-G

69547745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12840475-C-T

http://identifiers.org/hco/8/GRCh38#69547763-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12840493-C-A

69547763-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12840493-C-G

69547763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12840493-C-T

http://identifiers.org/hco/8/GRCh38#69548066-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12840811-C-A

69548978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12841254-A-G

69550575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12842903-A-G

69550630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12842940-G-A

69550682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12842991-G-A

69550795-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12843111-T-G

http://identifiers.org/hco/8/GRCh38#69551201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12844819-C-A

69551236-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12844845-G-C

69551266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12844855-T-C

69551319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12844909-G-A

69551319-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12844909-G-C

69551610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12845168-T-C

http://identifiers.org/hco/8/GRCh38#69552259-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12845461-A-C

69552337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12845543-A-G

69552428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12845640-C-T

69553499-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12845947-A-T

69553584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12846031-C-T

69554018-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12846525-T-G

69554100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12846607-G-A

http://identifiers.org/hco/8/GRCh38#69554230-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12846741-C-A

69554230-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12846741-C-G

69554336-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12846853-T-G

69555113-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12847615-G-C

69556082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12848967-G-A

69556097-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12848982-T-A

69556173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12849038-T-C

69556235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12849093-C-T

69556312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12849172-T-C

69556633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12849525-G-A

69559092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12850944-G-A

69559092-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12850944-G-C

69559179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12851012-T-C

69559250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12851072-A-G

69559393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12851147-C-T

69559516-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12851297-A-T

69559798-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12851552-A-T

69559799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12851553-G-A

69559806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12851560-G-A

69559988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12851698-T-C

69560197-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12851989-G-T

69560320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12852123-G-A

69560520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12852297-C-T

69560560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12852337-A-G

69560698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12852484-C-T

69560791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12852590-G-A

69561494-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12854358-T-G

69561655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12854470-G-A

http://identifiers.org/hco/8/GRCh38#69561756-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12854558-A-C

69561856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12854673-T-C

69561993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12854808-G-A

69562168-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12855085-G-T

69562260-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12855174-T-A

69562260-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12855174-T-G

69562687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12855565-G-A

http://identifiers.org/hco/8/GRCh38#69562693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12855571-C-A

http://identifiers.org/hco/8/GRCh38#69562766-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12855644-C-A

69562767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12855645-A-G

69562812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12855693-T-C

69562813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12855694-G-A

69562813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12855694-G-T

69562825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12855706-T-C

http://identifiers.org/hco/8/GRCh38#69562897-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12855778-C-A

69562897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12855778-C-T

69562906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12855788-G-A

69562912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12855793-A-G

69562959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12855821-C-T

69562980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12855836-A-G

69563090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12855950-A-G

69563175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12856032-G-A

69563175-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12856032-G-C

69563175-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12856032-G-T

69563235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12856059-C-T

69563237-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12856061-G-T

69563262-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12856082-C-G

69563262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12856082-C-T

69563438-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12856213-A-T

69563453-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12856216-T-A

http://identifiers.org/hco/8/GRCh38#69563531-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12856295-C-A

69563531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 12856295-C-T

69563644-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12856408-G-T

69563688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12856452-G-T

69563856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12856618-G-A

69563862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12856624-G-A

69563862-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12856624-G-T

69563898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12856655-T-C

69563943-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 12856718-T-G

69564101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 12856876-A-G

69564279-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12857062-T-A

69564873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12857964-C-T

http://identifiers.org/hco/8/GRCh38#69565182-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12858183-A-C

69565194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12858195-T-C

69565200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12858201-C-T

69565244-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12858236-G-T

69565248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12858240-A-G

69565248-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12858240-A-T

http://identifiers.org/hco/8/GRCh38#69565261-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12858253-C-A

69565261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12858253-C-T

69565368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12858348-G-A

69565520-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12858389-A-T

69565527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12858396-A-G

69565840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12858646-T-C

69565929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12858727-G-A

69566070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12858789-G-A

69566169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12858879-C-T

http://identifiers.org/hco/8/GRCh38#69566170-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12858880-C-A

69566170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12858880-C-T

69566321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12859020-A-G

69566508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12859189-A-G

69566941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12859319-G-A

69567004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12859369-A-G

69567092-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12859456-A-G

69567173-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12859551-T-A

69567291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12859640-T-C

69567309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12859658-A-G

69567367-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12859698-C-G

69568028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12860540-C-T

69568043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12860548-T-C

69568592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12861041-A-G

69568836-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12861386-C-G

69568878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12861432-T-C

69569087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12861677-A-G

69569104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12861688-C-T

http://identifiers.org/hco/8/GRCh38#69569122-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12861704-A-C

69569122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12861704-A-G

69569122-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12861704-A-T

http://identifiers.org/hco/8/GRCh38#69569135-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12861717-C-A

69569136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12861718-A-G

69569152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12861733-C-T

69569674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12862330-C-T

69569696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12862352-G-A

69569700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12862356-G-A

69569899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12862571-C-T

69569940-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12862635-A-T

69569952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12862641-C-T

69570042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12862735-A-G

69571354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12863474-C-T

69571417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12863527-C-T

http://identifiers.org/hco/8/GRCh38#69571884-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12863876-A-C

69572206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12864151-A-G

69572312-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12864231-G-T

http://identifiers.org/hco/8/GRCh38#69572321-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12864240-A-C

69572625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12864520-A-G

69572648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12864543-G-A

69573413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12864747-G-T

69573480-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12864813-A-T

69573499-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12864839-T-G

69573510-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12864850-T-A

69573575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12865124-T-C

69573817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12865330-G-A

69574078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12865541-C-T

69574167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12865594-C-T

69574212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12865638-C-T

69574802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12865936-G-T

69574828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12865958-C-T

69574866-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12865996-T-G

69574960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12866017-T-C

69575099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12866149-G-A

69575192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12866246-C-T

69575220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12866267-C-T

69575222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12866269-C-T

69575254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12866305-G-A

69575282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12866329-A-G

69575347-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12866369-G-T

69575531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12866583-G-A

69575933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12866953-G-A

http://identifiers.org/hco/8/GRCh38#69576124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12867144-C-A

69576124-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 12867144-C-G

69576124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 12867144-C-T

69576136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 12867156-T-C

69576373-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12868152-G-C

69576733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12868470-G-A

69576881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12868599-G-A

69576887-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12868605-A-T

69576896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12868614-T-C

69576912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12868631-A-G

69577160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12868868-C-T

69577437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12869128-G-A

69577462-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12869552-G-T

69577727-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12869827-T-A

69577812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12869905-T-C

69578173-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12870378-G-C

69578173-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12870378-G-T

69579833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12870702-G-A

69580460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12871308-C-T

69580666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12871466-T-C

69580702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12871500-A-G

69580738-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12871534-A-T

http://identifiers.org/hco/8/GRCh38#69580829-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12871647-A-C

69580992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12871840-A-G

69581037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12871885-A-G

69581218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12872049-G-A

69581240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12872058-T-C

69581281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12872096-T-C

http://identifiers.org/hco/8/GRCh38#69581283-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12872098-C-A

69581501-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12872314-T-A

69581717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12872509-C-T

69581745-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12872537-G-C

69581778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12872570-C-T

69581797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12872591-G-A

69581797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12872591-G-T

69581836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12872620-A-G

69581938-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12872704-G-C

69582110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12872867-A-G

69582461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12873092-T-C

69582471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12873102-G-A

69582481-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12873112-T-A

69582554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12873179-G-A

69582659-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12873245-T-G

69582692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12873275-A-G

69582729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12873317-G-A

69582729-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12873317-G-C

69582763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12873345-G-A

69582763-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12873345-G-T

69582881-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12873460-A-T

69582889-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12873468-G-C

69583892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12874816-G-A

69583892-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12874816-G-T

69585888-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12874949-A-T

69585894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12874955-G-A

69585911-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12874972-T-G

69586029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12875096-T-C

69586234-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12875283-T-A

69586234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12875283-T-C

69586300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12875347-A-G

69586300-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12875347-A-T

69586529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12875572-C-T

69586568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12875613-A-G

69586568-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12875613-A-T

69586593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12875638-A-G

69586593-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12875638-A-T

http://identifiers.org/hco/8/GRCh38#69586605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12875650-C-A

69586624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12875669-G-A

69586624-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12875669-G-T

69586641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12875686-G-A

69586641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12875686-G-T

69586724-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12875778-A-T

http://identifiers.org/hco/8/GRCh38#69586746-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12875800-A-C

69586763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12875817-T-C

69586823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12875863-G-A

69586877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12875904-G-A

69586945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12875970-T-C

http://identifiers.org/hco/8/GRCh38#69587336-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12876474-C-A

69587402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12876539-G-A

69587402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12876539-G-T

69587573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12876705-G-A

69587659-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12876798-A-T

69587744-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12876868-T-G

69587902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12877049-G-A

69588151-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12877300-T-A

69588209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12877368-C-T

69588212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12877371-C-T

69588344-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12877513-G-T

69588623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12877744-G-A

http://identifiers.org/hco/8/GRCh38#69588698-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12877820-C-A

69589082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 12878188-C-T

69589177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12878283-A-G

69589177-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12878283-A-T

69589179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12878285-G-A

69589205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12878310-T-C

http://identifiers.org/hco/8/GRCh38#69589206-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12878311-C-A

http://identifiers.org/hco/8/GRCh38#69589242-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12878347-C-A

http://identifiers.org/hco/8/GRCh38#69589243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12878348-C-A

69589243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12878348-C-T

69589247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12878352-A-G

69589255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12878376-T-C

69589259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12878380-T-C

http://identifiers.org/hco/8/GRCh38#69589282-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12878403-C-A

69589282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12878403-C-T

69589286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12878407-G-A

69589286-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12878407-G-C

69589300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12878421-C-T

69589301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12878422-G-A

69589334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12878456-G-A

69589432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12878547-T-C

69589586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12878709-G-A

69589771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12878877-G-A

69590075-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12879119-G-C

69590561-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12879299-G-C

69590759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12879424-C-T

http://identifiers.org/hco/8/GRCh38#69590805-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12879454-C-A

69590810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12879459-C-T

69590813-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12879462-G-C

69590878-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12879524-G-C

http://identifiers.org/hco/8/GRCh38#69590940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12879586-C-A

69590940-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12879586-C-G

69591014-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12879668-G-C

69591206-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12879833-A-T

69591244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12879879-A-G

69591807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12880036-A-G

69591970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12880147-G-A

69592061-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12880235-C-G

69592130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12880404-G-A

69592130-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12880404-G-C

69592139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12880442-T-C

69592142-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12880445-G-T

69592193-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12880547-C-G

69592193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12880547-C-T

69592359-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12880725-T-G

69592399-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12880757-A-T

69592458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12880815-G-A

69592698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12881020-C-T

69592879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12881194-T-C

69593101-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12881396-T-A

69593234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12881531-G-A

69593251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12881548-C-T

69594724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12882672-T-C

69594727-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12882675-G-T

http://identifiers.org/hco/8/GRCh38#69594740-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12882688-C-A

69595255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12883157-C-T

69595281-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12883183-C-G

69595418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12883311-C-T

69595461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12883354-G-A

69595852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12883721-A-G

69596172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12884088-A-G

http://identifiers.org/hco/8/GRCh38#69597101-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12884599-C-A

69597283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12884775-A-G

http://identifiers.org/hco/8/GRCh38#69597293-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12884784-C-A

69597405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12884909-A-G

69597673-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12885173-T-A

69597811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12885309-A-G

69597823-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12885321-T-G

http://identifiers.org/hco/8/GRCh38#69597882-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12885380-C-A

69597899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12885397-T-C

69598047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12885570-A-G

69598126-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12885640-G-C

69598126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12885640-G-T

http://identifiers.org/hco/8/GRCh38#69598148-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12885662-C-A

http://identifiers.org/hco/8/GRCh38#69598210-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12885775-A-C

69598210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12885775-A-G

69599226-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12886249-T-G

69599330-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12886352-T-A

69599422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12886410-A-G

69599463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12886454-G-A

69599565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12886538-G-A

69599565-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12886538-G-C

69599707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12886629-A-G

69599803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12886700-G-A

69599995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12886936-G-A

69600003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12886944-G-A

69600105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12887060-G-A

69600105-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12887060-G-C

69600146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12887100-A-G

http://identifiers.org/hco/8/GRCh38#69600535-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12887476-C-A

69600609-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 12887568-T-G

69600702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 12887661-A-G

69600814-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12887757-T-A

69600814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12887757-T-C

http://identifiers.org/hco/8/GRCh38#69600821-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12887764-C-A

69600901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12887816-G-A

69600901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12887816-G-T

69600991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12887877-A-G

69601497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12888336-A-G

69601574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12888535-G-A

69601574-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12888535-G-T

69601577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12888538-G-A

69601629-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12888580-G-T

69601645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12888593-G-A

http://identifiers.org/hco/8/GRCh38#69601654-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12888602-C-A

69601677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 12888625-G-A

69601713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 12888661-C-T

69601854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12888798-T-C

69602077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12888974-A-G

69602130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12889025-C-T

http://identifiers.org/hco/8/GRCh38#69602149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12889042-C-A

69602149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12889042-C-T

69602150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12889043-G-A

69602150-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12889043-G-T

69603039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12890476-C-T

69603064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12890491-G-T

69603252-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 12890685-C-G

69603252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 12890685-C-T

69603312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 12890745-A-G

69603343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12890776-A-G

69603406-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12890825-G-C

69603494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12890913-A-G

http://identifiers.org/hco/8/GRCh38#69603569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12890988-C-A

69603683-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12891101-T-A

69603683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12891101-T-C

http://identifiers.org/hco/8/GRCh38#69603689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12891107-C-A

69603689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12891107-C-T

http://identifiers.org/hco/8/GRCh38#69603690-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12891108-C-A

69603690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12891108-C-T

69603755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12891175-G-A

69603778-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12891198-A-T

69604180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12891493-A-G

69604261-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12891570-A-T

69604402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12891660-A-G

69604484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12891732-G-A

69604621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12892021-T-C

69604621-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12892021-T-G

69604742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12892136-G-A

69604742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12892136-G-T

69604784-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12892175-T-G

69604789-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12892180-C-G

69605024-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12892397-G-T

69605044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12892415-G-A

69605080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12892449-G-A

69605080-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12892449-G-T

69605094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12892463-G-A

69605094-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12892463-G-T

69605191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12892556-G-T

69605281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12892617-G-A

69605313-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12892649-G-C

69605319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12892655-T-C

69605348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12892679-A-G

69605446-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12892758-G-T

http://identifiers.org/hco/8/GRCh38#69605476-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12892786-A-C

69605512-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12892801-T-C

69605513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12892802-A-G

69606062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12894095-A-G

69606110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12894137-A-G

69606113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12894140-C-T

69606151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12894179-C-T

69606221-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12894233-T-A

69606221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12894233-T-C

69606267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12894272-A-G

69606528-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12894513-C-G

69606559-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12894546-C-G

69606559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12894546-C-T

http://identifiers.org/hco/8/GRCh38#69606577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12894564-C-A

69606593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12894584-G-A

69606808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12895198-C-T

69606820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12895210-T-C

69606891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12895279-G-A

69606923-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12895312-G-C

69606924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12895313-C-T

69607140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12895545-C-T

69607141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12895546-A-G

69607720-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12895725-G-T

69607723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12895728-A-G

69607988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12896042-A-G

69607999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12896053-C-T

69608044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12896094-A-G

69608149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12896197-C-T

69608272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12896290-A-G

69608770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12896433-C-T

69608778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12896441-G-A

69608778-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12896441-G-C

69608904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12896566-G-A

69608943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12896601-G-A

69611082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12896925-C-T

69611411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12897190-C-T

69611450-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12897229-A-T

69611462-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12897235-A-T

http://identifiers.org/hco/8/GRCh38#69611484-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12897252-C-A

69611484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12897252-C-T

69611632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12897387-G-A

69611632-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12897387-G-C

69611632-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12897387-G-T

69611784-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12897528-G-T

69613591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12897834-G-A

69613658-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12897890-G-T

69613686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12897918-G-A

69614523-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12901807-T-G

69614799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12902067-T-C

http://identifiers.org/hco/8/GRCh38#69614912-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12902188-C-A

69614917-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12902196-A-T

69615372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12902590-G-A

69616995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12903586-G-A

69617159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12903735-T-C

69617764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12903939-A-G

69618103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12904236-C-T

69618168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12904307-A-G

69618727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12904771-G-A

69618880-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12904916-T-A

69618897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12904933-T-C

69619415-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12905522-T-G

69620919-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12906186-A-T

69621124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 12906426-G-A

http://identifiers.org/hco/8/GRCh38#69621279-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12906581-A-C

69621279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12906581-A-G

69621285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12906587-G-A

69621285-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12906587-G-C

69621285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12906587-G-T

69621291-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12906593-G-T

69621342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12906662-T-C

69621358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12906678-A-G

69621376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12906696-G-A

69621376-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12906696-G-T

http://identifiers.org/hco/8/GRCh38#69621389-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12906711-C-A

69621389-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12906711-C-G

69621487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12906808-T-C

69621487-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12906808-T-G

69621844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12907162-T-C

http://identifiers.org/hco/8/GRCh38#69621890-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12907206-A-C

69621916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12907231-T-C

69621942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12907252-T-C

69621943-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12907253-T-G

69622924-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12907698-G-C

69622953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12907734-C-T

69623002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12907778-G-A

69623002-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12907778-G-C

69623138-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12907899-G-C

69623138-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12907899-G-T

69623141-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12907902-C-G

69623141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12907902-C-T

http://identifiers.org/hco/8/GRCh38#69623146-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12907907-A-C

http://identifiers.org/hco/8/GRCh38#69623150-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12907911-C-A

69623217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12907976-T-C

69623244-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12908002-T-A

69623335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12908099-C-T

69623832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12908476-G-A

69623832-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12908476-G-T

69623873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12908516-G-A

69623873-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12908516-G-C

69623988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 12908629-C-T

69624101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 12908739-G-A

69624174-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 12908812-T-A

69624329-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12908962-T-A

69624329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12908962-T-C

69627116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12909954-G-A

http://identifiers.org/hco/8/GRCh38#69627185-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12910029-C-A

69627185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12910029-C-T

69627355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12910252-G-A

69627355-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12910252-G-C

69627355-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12910252-G-T

69627444-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12910350-T-A

69627444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12910350-T-C

69627444-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12910350-T-G

http://identifiers.org/hco/8/GRCh38#69627535-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12910429-C-A

69627535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12910429-C-T

69627571-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12910452-C-G

69627642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12910498-T-C

http://identifiers.org/hco/8/GRCh38#69627661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12910516-C-A

69627678-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12910540-T-A

69627678-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12910540-T-G

69627687-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12910549-A-T

69627689-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12910551-A-T

http://identifiers.org/hco/8/GRCh38#69627716-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12910573-C-A

69627716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12910573-C-T

http://identifiers.org/hco/8/GRCh38#69627752-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12910607-C-A

69627756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12910611-A-G

http://identifiers.org/hco/8/GRCh38#69627760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12910615-C-A

69627760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12910615-C-T

69627850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 12910705-A-G

http://identifiers.org/hco/8/GRCh38#69627861-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12910716-A-C

69627873-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 12910728-T-A

http://identifiers.org/hco/8/GRCh38#69628115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12911607-C-A

69628123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12911615-T-C

http://identifiers.org/hco/8/GRCh38#69628125-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12911617-C-A

69628178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 12911674-A-G

http://identifiers.org/hco/8/GRCh38#69628245-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12911741-C-A

69628245-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12911741-C-G

http://identifiers.org/hco/8/GRCh38#69628829-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12912573-A-C

http://identifiers.org/hco/8/GRCh38#69628831-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12912575-C-A

69628831-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12912575-C-G

http://identifiers.org/hco/8/GRCh38#69628973-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12912706-C-A

69628973-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12912706-C-G

69628986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12912717-A-G

http://identifiers.org/hco/8/GRCh38#69629390-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12912802-C-A

69629390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12912802-C-T

69629393-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12912803-T-G

69629418-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12912814-T-G

69629423-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12912819-G-T

69629427-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12912823-G-T

69629477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12912869-T-C

69629576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 12912945-G-A

http://identifiers.org/hco/8/GRCh38#69629719-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12913076-C-A

69629719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12913076-C-T

69629729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12913089-G-A

69629729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12913089-G-T

http://identifiers.org/hco/8/GRCh38#69629779-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12913148-A-C

69630669-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12914473-T-G

69630767-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12914547-A-T

69638218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12918064-A-G

69638267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12918114-A-G

69638267-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12918114-A-T

69638493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12918310-A-G

http://identifiers.org/hco/8/GRCh38#69638495-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12918312-C-A

69638495-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 12918312-C-G

69638495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 12918312-C-T

69638572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 12918389-G-A

69638655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12918472-A-G

69638900-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12918710-T-G

69639092-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12918910-A-G

69639156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12918973-C-T

69639355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12919158-C-T

69639533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12919320-C-T

69639615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12919398-G-A

69640008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12920365-C-T

69640216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12920466-G-A

http://identifiers.org/hco/8/GRCh38#69640297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12920548-C-A

69640305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12920560-G-T

69640415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12920655-C-T

69640597-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12920776-A-T

69640600-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12920779-T-G

69640601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12920780-T-C

69640601-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12920780-T-G

69640617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12920796-C-T

http://identifiers.org/hco/8/GRCh38#69640687-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12920868-C-A

http://identifiers.org/hco/8/GRCh38#69640700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12920881-C-A

69640700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12920881-C-T

69640703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12920884-G-A

69640703-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12920884-G-C

69640703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12920884-G-T

http://identifiers.org/hco/8/GRCh38#69640732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12920912-C-A

69640958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12921132-G-A

69640958-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12921132-G-T

http://identifiers.org/hco/8/GRCh38#69641029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12921202-C-A

69641097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12921274-C-T

http://identifiers.org/hco/8/GRCh38#69641150-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12921324-C-A

69641197-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12921353-G-T

69641258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12921418-G-A

69641258-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12921418-G-T

69641439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12921596-A-G

69643889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12922252-A-G

69643968-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12922333-C-G

69648880-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12922721-T-G

69649165-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12923192-T-A

69649250-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12923271-G-T

69649327-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12923342-A-T

69649402-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12923410-T-G

69649617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12923619-T-C

69657386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12927944-G-A

69657597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12928121-G-A

69657601-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12928125-T-G

69657640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12928168-T-C

http://identifiers.org/hco/8/GRCh38#69658092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12928537-C-A

http://identifiers.org/hco/8/GRCh38#69658470-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12929001-C-A

69658511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 12929042-G-A

http://identifiers.org/hco/8/GRCh38#69658546-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12929077-C-A

69658546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 12929077-C-T

69658589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 12929120-G-A

69658796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 12929324-C-T

69658890-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 12929418-A-T

69658920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 12929448-T-C

http://identifiers.org/hco/8/GRCh38#69659000-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12929528-A-C

69659070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 12929601-G-A

69659070-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 12929601-G-T

http://identifiers.org/hco/8/GRCh38#69659077-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#12929608-C-A

69659077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 12929608-C-T

69659104-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 12929635-T-G

69659110-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 12929641-G-C

69659449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 12929991-T-C

69659503-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 12930041-C-G

69659524-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 12930058-G-T

69659703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 12930220-A-G

69660260-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 12930762-T-G

69660421-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 12930923-G-T

69660461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 12930961-T-C

69660657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 12931156-A-G

69660739-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20391
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 12931234-A-T