126326918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 5 prime UTR variant
orthologous variants: 33777416-G-A

126326918-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 5 prime UTR variant
orthologous variants: 33777416-G-C

126326918-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 5 prime UTR variant
orthologous variants: 33777416-G-T

126326948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: missense variant
orthologous variants: 33777386-G-A

126326948-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: missense variant
orthologous variants: 33777386-G-C

126326948-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: missense variant
orthologous variants: 33777386-G-T

126327306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33777093-G-A

126327570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, undefined
orthologous variants: 33776912-G-T

http://identifiers.org/hco/9/GRCh38#126328299-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33776258-C-A

126328299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33776258-C-T

126329103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33775724-G-A

126329419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33775465-T-C

126329796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33775086-T-C

126329945-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33774974-G-T

126330062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33774869-C-T

126330283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33774645-T-C

http://identifiers.org/hco/9/GRCh38#126330348-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33774546-A-C

http://identifiers.org/hco/9/GRCh38#126330361-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33774525-C-A

http://identifiers.org/hco/9/GRCh38#126330723-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33772896-A-C

126330723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33772896-A-G

126331164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33772515-T-C

126331187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33772492-T-C

126331211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33772470-A-G

126331266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33772417-G-A

126331266-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33772417-G-C

126331271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33772410-G-A

126331271-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33772410-G-T

126331515-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33772176-A-T

126331518-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33772173-T-G

126331547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33772133-T-C

http://identifiers.org/hco/9/GRCh38#126331559-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33772121-C-A

126331657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33772022-C-T

126331665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33772014-T-C

126331744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33771935-G-A

126331910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33771821-G-A

126331981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33771758-G-A

126332104-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33771651-G-C

126332193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33771602-C-T

126332310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33771511-C-T

http://identifiers.org/hco/9/GRCh38#126332506-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33771337-C-A

126332506-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33771337-C-G

126332825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33771080-T-C

126332911-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33771012-C-G

126332936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33770993-G-A

126333001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33770935-A-G

126333940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33770656-A-G

126333944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33770652-T-C

126334043-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33770547-G-C

126334043-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33770547-G-T

126334506-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33770212-C-G

126334552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33770174-G-A

126334559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33770167-C-T

126334789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, undefined
orthologous variants: 33769947-C-T

126334804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, undefined
orthologous variants: 33769932-G-A

126334814-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33769922-G-C

http://identifiers.org/hco/9/GRCh38#126335107-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#33769675-C-A

126335107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, undefined
orthologous variants: 33769675-C-T

126335115-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, undefined
orthologous variants: 33769667-G-T

http://identifiers.org/hco/9/GRCh38#126335166-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#33769617-C-A

http://identifiers.org/hco/9/GRCh38#126335250-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#33769531-C-A

126335250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 33769531-C-T

126335400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, missense_variant
orthologous variants: 33769389-C-T

126335561-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33769289-G-C

126335637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33769227-T-C

126335642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33769222-G-A

126335660-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33769199-T-G

126335958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33768928-C-T

126336031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33768850-G-A

126336297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33768673-A-G

126336317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33768653-T-C

126336414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33768567-C-T

126336415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33768566-A-G

126336536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33768428-G-A

126337650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33767388-C-T

126338034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33766951-G-A

126338274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33766686-T-C

http://identifiers.org/hco/9/GRCh38#126338326-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33766627-C-A

126338326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33766627-C-T

126338327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33766626-A-G

126338530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33766409-G-T

http://identifiers.org/hco/9/GRCh38#126338569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33766361-C-A

126338968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33765953-T-C

126339082-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33765910-G-T

126339723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33765323-A-G

126340183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33764778-G-A

126340321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33764641-G-A

126340562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: missense variant
orthologous variants: 33764416-T-C

126340583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: missense variant
orthologous variants: 33764395-G-A

126340592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: missense variant
orthologous variants: 33764386-G-A

http://identifiers.org/hco/9/GRCh38#126340641-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33764337-A-C

126340654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33764324-C-T

http://identifiers.org/hco/9/GRCh38#126340722-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33764288-A-C

126340722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33764288-A-G

126340722-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33764288-A-T

126340741-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33764269-G-C

126340768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33764229-G-A

126340768-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33764229-G-T

126340777-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33764220-T-A

126340777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33764220-T-C

126342257-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33763515-T-A

126342258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33763514-C-T

126342395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33763392-T-C

126342512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33763276-A-G

126342728-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33763076-G-T

126346966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33761955-G-A

126346993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33761932-G-A

http://identifiers.org/hco/9/GRCh38#126347207-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33761717-C-A

126347245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33761680-C-T

126347279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33761646-A-G

126347308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33761599-C-T

126348040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33760924-C-T

http://identifiers.org/hco/9/GRCh38#126363839-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33743481-C-A

126363839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33743481-C-T

126364414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33743039-C-T

126364424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33743029-C-T

126364554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33742939-A-G

126365700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33742667-A-G

126366837-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33741254-C-G

126366855-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33741236-C-G

126370863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33738798-A-G

126371061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33738677-G-A

126371281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33738477-G-A

126371653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33738231-C-T

126372196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33737813-T-C

126372197-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33737812-T-G

126372838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33737271-C-T

http://identifiers.org/hco/9/GRCh38#126372847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33737262-C-A

126372847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33737262-C-T

126373098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33737088-A-G

126373439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33736818-A-G

126373579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33736683-C-T

126373589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33736674-A-G

126373653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33736642-A-G

126373678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33736629-G-A

126373834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33736498-C-T

126374508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33733307-A-G

126377522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33732117-G-A

126377526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33732113-C-T

126378005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33731728-G-T

http://identifiers.org/hco/9/GRCh38#126378020-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33731713-A-C

126378111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33731626-G-A

126379687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33731377-T-C

126380017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33731172-C-T

126380069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33731123-A-G

http://identifiers.org/hco/9/GRCh38#126380558-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33730785-A-C

126380681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33730675-C-T

126380924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33730427-G-A

126380924-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33730427-G-T

http://identifiers.org/hco/9/GRCh38#126380950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33730401-C-A

126380950-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33730401-C-G

126380950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33730401-C-T

126380983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33730368-G-A

126380983-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33730368-G-T

http://identifiers.org/hco/9/GRCh38#126381001-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33730349-C-A

126381001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33730349-C-T

126381046-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33730294-T-G

126381065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 33730275-T-C

126381204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33730136-G-A

126381204-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33730136-G-C

126381204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33730136-G-T

http://identifiers.org/hco/9/GRCh38#126381207-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33730133-C-A

126381208-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33730132-A-T

126381323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33730021-G-A

126381564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33729796-A-G

http://identifiers.org/hco/9/GRCh38#126383181-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33727535-C-A

126383871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33726826-C-T

126383969-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33726737-A-T

126384013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33726694-C-T

126384190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33726516-C-T

126384349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33726387-G-A

126384510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33726246-C-T

126385627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33725426-A-G

126385958-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33725116-A-T

http://identifiers.org/hco/9/GRCh38#126386443-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33724754-C-A

126386443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33724754-C-T

126386464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33724733-G-A

126386464-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33724733-G-T

126386497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33724700-A-G

http://identifiers.org/hco/9/GRCh38#126386730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33724480-C-A

126386730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33724480-C-T

http://identifiers.org/hco/9/GRCh38#126386765-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33724459-C-A

126386810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33724423-T-C

126386810-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33724423-T-G

126387038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33724172-G-A

126388877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33720591-C-T

126389025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33720448-C-T

126389235-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33720324-A-T

126389297-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33720285-G-C

126389297-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33720285-G-T

126389469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33720112-A-G

http://identifiers.org/hco/9/GRCh38#126389566-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33720014-C-A

126389566-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33720014-C-G

126389916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33719785-A-G

126391642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33718179-C-T

126391945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33717909-A-G

126391945-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33717909-A-T

http://identifiers.org/hco/9/GRCh38#126391960-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33717895-C-A

126391960-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33717895-C-G

126391960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33717895-C-T

http://identifiers.org/hco/9/GRCh38#126391961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33717894-C-A

126391971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33717884-G-A

126391971-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33717884-G-T

126391996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33717870-T-C

126392031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33717854-A-G

http://identifiers.org/hco/9/GRCh38#126392038-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33717847-A-C

126392092-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: missense variant
orthologous variants: 33717795-C-G

126392107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: missense variant
orthologous variants: 33717780-A-G

http://identifiers.org/hco/9/GRCh38#126392146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33717741-C-A

126392146-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: missense variant
orthologous variants: 33717741-C-G

126392146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: missense variant
orthologous variants: 33717741-C-T

126392183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: missense variant
orthologous variants: 33717704-A-G

126392376-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33717539-C-G

126392376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33717539-C-T

126392476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33717461-T-C

126392544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33717394-G-A

126392544-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33717394-G-T

126393089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33717055-G-A

126393094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33717050-T-C

126393268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33716902-C-T

126393355-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33716830-C-G

126393355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33716830-C-T

126394475-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33716025-G-C

126394475-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33716025-G-T

126394647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33715884-G-A

126394661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33715870-A-G

http://identifiers.org/hco/9/GRCh38#126394883-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33715672-A-C

126394963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33715603-T-C

126394973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33715593-G-A

126395058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33715507-T-C

126395103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33715463-C-T

126395352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33715378-C-T

http://identifiers.org/hco/9/GRCh38#126395483-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#33715269-C-A

126395483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, undefined
orthologous variants: 33715269-C-T

126395499-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, undefined
orthologous variants: 33715258-G-T

126395500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, undefined
orthologous variants: 33715257-A-G

http://identifiers.org/hco/9/GRCh38#126395642-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#33715113-C-A

126395648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 33715107-A-G

126395681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 33715074-G-A

126395681-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 33715074-G-C

126395865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 33714886-T-C

126395993-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 33714411-A-T

126395997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 33714407-G-T

http://identifiers.org/hco/9/GRCh38#126396052-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33714360-C-A

126396284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 33714200-A-G

http://identifiers.org/hco/9/GRCh38#126396424-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33714073-C-A

126396424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 33714073-C-T

126396575-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 33713931-G-T

126396669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 33713845-G-A

126396669-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 33713845-G-C

126396669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 33713845-G-T

126396751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 33713792-G-A

126396751-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 33713792-G-C

126396751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 33713792-G-T

126396874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 33713768-C-T

126396875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 33713767-T-C

http://identifiers.org/hco/9/GRCh38#126396909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33713734-C-A

126396934-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 33713705-G-T

126396939-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 33713700-A-G

126397040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 33713597-G-A

126397040-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 33713597-G-T

126397082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 33713589-G-A

126397082-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 33713589-G-T

126397083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 33713588-G-A

126397083-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 33713588-G-T

126397279-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 33713085-G-T

126397294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 33713070-G-A

126397294-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 33713070-G-T

126397400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33712981-G-A

126397400-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33712981-G-T

126397427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33712954-T-C

126397437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 33712944-A-G

126397627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 33712771-G-T

126397666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33712727-G-A

126397666-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33712727-G-C

126397667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33712726-A-G

126397669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33712724-G-A

126397670-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33712723-C-G

126397670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33712723-C-T

http://identifiers.org/hco/9/GRCh38#126397690-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33712701-C-A

126397690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33712701-C-T

126397700-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33712691-T-A

126397752-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33712631-T-A

126397762-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33712621-T-A

126397853-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33712532-C-G

http://identifiers.org/hco/9/GRCh38#126398059-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33712335-C-A

126398190-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33712224-T-A

126398222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33712210-C-T

126399191-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33711394-T-A

126399302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33711321-C-T

126399323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33711299-C-T

126399333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33711290-C-T

126399342-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33711281-C-G

126399342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33711281-C-T

126399399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33711226-C-T

126399443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33711183-C-T

126399458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33711130-G-A

126399514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33711071-A-G

126399621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33710937-G-A

126399846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33710744-G-A

126399846-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33710744-G-C

126399992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33710596-A-G

126401363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33708490-C-T

126402324-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33707537-C-G

126404629-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33706461-T-G

126404777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33706310-G-A

http://identifiers.org/hco/9/GRCh38#126404784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33706303-C-A

126405406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33705745-A-G

126405516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33705638-T-C

126405533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33705621-C-T

126405657-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33705518-G-T

126405678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33705497-G-T

126405963-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33705249-T-G

126406172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33705118-C-T

126406174-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33705116-G-C

http://identifiers.org/hco/9/GRCh38#126406311-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33704976-C-A

http://identifiers.org/hco/9/GRCh38#126406428-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33704861-A-C

126406734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33704576-C-T

126406843-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33704471-T-A

126406881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33704434-A-G

126406930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33704396-A-G

126407132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33704223-A-G

126407192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33704192-A-G

126407431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33703972-C-T

126407534-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33703860-C-G

126407608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33703784-T-C

http://identifiers.org/hco/9/GRCh38#126407621-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33703771-A-C

126407671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33703723-A-G

126407933-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33703438-G-T

126407957-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33703421-G-T

126408143-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33703234-G-T

126408148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33703229-G-A

126408459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33702910-G-A

126408459-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33702910-G-T

126408472-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33702897-G-T

126408490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33702858-T-C

http://identifiers.org/hco/9/GRCh38#126408492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33702856-C-A

126408564-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33702792-C-G

126408628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33702728-C-T

126410025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33701541-C-T

http://identifiers.org/hco/9/GRCh38#126410454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33701205-C-A

126410458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33701201-A-G

126410533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33701147-C-T

126410622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33701074-C-T

126411669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33700316-G-A

126411699-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33700296-T-A

126411699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33700296-T-C

126411869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33700139-C-T

126411958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33700066-A-G

126413006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33699182-G-A

126413118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33699082-C-T

126413328-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33698911-T-C

126413469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33698771-C-T

126413569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33698689-A-G

http://identifiers.org/hco/9/GRCh38#126413872-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33696914-A-C

126413872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33696914-A-G

126413881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33696905-G-A

126413881-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33696905-G-C

126414407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33696402-T-C

126415612-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33695687-G-C

126417255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33694028-C-T

126417327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33693962-A-G

126417409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33693870-C-T

126420977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33693512-G-A

126421020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33693470-C-T

126421064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33693426-T-C

126421090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33693403-A-G

126421094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33693399-G-A

http://identifiers.org/hco/9/GRCh38#126421514-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33693096-C-A

126421514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33693096-C-T

126421698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33693003-G-A

126421707-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33692994-T-G

126421807-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33692897-G-C

http://identifiers.org/hco/9/GRCh38#126421843-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33692860-C-A

126421843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33692860-C-T

126421933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 33692770-T-C

126421962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33692742-C-T

http://identifiers.org/hco/9/GRCh38#126422097-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33692673-C-A

126422097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33692673-C-T

126422197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33692592-T-C

126422197-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33692592-T-G

126422213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33692590-G-A

126422259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33692549-C-T

126422645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33692254-G-A

126423186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33691719-C-T

126423355-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33691568-C-G

126423432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33691499-C-T

126423645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33691293-A-G

126424622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33690473-A-G

126425109-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33689995-T-G

http://identifiers.org/hco/9/GRCh38#126426496-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33689062-A-C

126426799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33688749-G-T

126426837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33688732-A-G

126426837-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33688732-A-T

http://identifiers.org/hco/9/GRCh38#126426864-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33688705-C-A

126426864-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33688705-C-G

http://identifiers.org/hco/9/GRCh38#126426871-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33688698-C-A

126426871-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33688698-C-G

126426890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33688686-G-A

126426925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33688654-A-G

http://identifiers.org/hco/9/GRCh38#126426948-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33688631-C-A

126426948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33688631-C-T

126427082-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33688516-G-T

126428072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33687674-T-C

126428721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33686948-C-T

126428759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33686924-A-G

126428761-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33686922-T-G

http://identifiers.org/hco/9/GRCh38#126429137-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33686611-A-C

126430076-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33685767-G-C

http://identifiers.org/hco/9/GRCh38#126430099-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33685738-C-A

126430121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33685716-G-A

126430121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33685716-G-T

126430163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33685673-G-T

126430221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33685608-T-C

126430283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33685554-C-T

126430286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33685551-G-A

126430286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33685551-G-T

126430916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33685105-C-T

126431151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33684871-A-G

126431496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33684529-A-G

http://identifiers.org/hco/9/GRCh38#126431696-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33684367-A-C

126431700-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33684363-G-C

126431735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33684328-G-A

126431865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33684234-A-G

126432033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33684148-C-T

126432097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33684089-C-T

126432370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33683904-C-T

126432700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33683581-C-T

126432933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33683389-C-T

126433349-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33683189-G-T

126433607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33682984-C-T

126434312-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33682336-G-T

126434545-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33682120-G-T

126435323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33681150-A-G

126435725-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33680813-G-C

126435776-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33680786-G-T

126436101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33680489-A-G

126436538-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33680091-G-T

http://identifiers.org/hco/9/GRCh38#126437138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33679469-C-A

126437138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33679469-C-T

126437851-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33678756-T-A

126437858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33678749-G-A

126438351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33678253-T-C

126438509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33678106-T-C

http://identifiers.org/hco/9/GRCh38#126438603-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33678065-A-C

126438708-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33677938-T-A

126438994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33677760-G-A

126439095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33677659-A-G

126439095-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33677659-A-T

http://identifiers.org/hco/9/GRCh38#126439186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33677578-C-A

126439697-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33677178-G-T

126440417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33676485-G-A

126441165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33675703-C-T

126441258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33675610-C-T

126441446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33675483-T-C

126442283-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33674779-C-G

126442424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33674639-G-A

126442461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33674605-T-C

126442752-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33674402-T-G

http://identifiers.org/hco/9/GRCh38#126442792-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33674354-A-C

126442802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33674344-G-A

126442905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33674259-C-T

126442932-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33674232-T-A

126442994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33674162-T-C

126443069-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33674097-T-G

126449616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33670081-C-T

126452379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: -C-T

126452380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: -G-A

126452381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: -G-A

126454209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33667303-G-A

126454411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33667136-T-C

126454432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33667115-A-G

126454433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33667114-T-C

126454463-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33667084-T-A

126454499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33667052-G-A

126456311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33666666-G-A

126456311-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33666666-G-T

126456369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33666608-A-G

126456381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33666596-A-G

126456565-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33666417-C-G

126456565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33666417-C-T

126456865-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33666114-T-G

126456926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33666038-T-C

126457067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33665938-C-T

126457075-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33665930-T-G

126457081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33665924-C-T

126457085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33665920-G-A

126457085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33665920-G-T

126457659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33665448-G-A

126457729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33665385-G-A

126457731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33665379-G-A

126457759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33665356-G-A

126457759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33665356-G-T

http://identifiers.org/hco/9/GRCh38#126457939-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33665174-A-C

http://identifiers.org/hco/9/GRCh38#126458058-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33665077-C-A

126458058-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33665077-C-G

126458071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33665064-C-T

126458107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33665028-C-T

126458580-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33664656-C-G

126458704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33664521-T-C

126458729-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33664496-G-C

126459220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33664007-C-T

126459386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33663941-A-G

126459730-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33663690-C-G

126459730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33663690-C-T

126459926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33663516-G-A

http://identifiers.org/hco/9/GRCh38#126460356-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33663175-A-C

126460360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33663171-T-C

126460943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33662878-C-T

126460990-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33662849-T-A

126461116-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33662737-T-C

126461160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33662699-G-A

126461160-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33662699-G-C

126461160-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33662699-G-T

http://identifiers.org/hco/9/GRCh38#126461186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33662673-C-A

126461186-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33662673-C-G

126461206-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33662648-T-A

126461817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33662070-G-A

126461828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33662061-G-A

126461870-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33662016-G-T

126463327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33660591-G-A

126463349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33660569-C-T

126463369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33660549-G-A

126463992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33659996-A-G

http://identifiers.org/hco/9/GRCh38#126464010-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33659975-C-A

126464010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33659975-C-T

126464170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33659859-G-A

126464523-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33659627-G-C

126464819-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33659409-T-G

126465024-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33659214-G-T

126465734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33658632-A-G

http://identifiers.org/hco/9/GRCh38#126465842-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33658537-C-A

http://identifiers.org/hco/9/GRCh38#126466040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33658453-C-A

126466165-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33658335-C-G

126466521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33658033-T-C

126466598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33657979-G-A

126466639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33657921-G-A

126469515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33652798-T-C

126469840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33652511-C-T

126470821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33651276-C-T

126470850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33651247-A-G

126471022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33651145-G-A

126471136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33651039-G-A

126471296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33650890-T-C

126471686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33650519-C-T

126471966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33650264-A-G

126472251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33650116-T-C

126472403-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33650024-T-G

http://identifiers.org/hco/9/GRCh38#126472484-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33649944-C-A

126473007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33649440-A-G

126473076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33649385-C-T

126473223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33649255-A-G

126473264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33649215-G-T

126473860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33649084-T-C

126474034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33648922-C-T

126474096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33648891-G-A

126474134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33648853-C-T

126474234-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33648787-A-T

126474282-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33648734-T-G

126474431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33648589-A-G

126474562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33648464-C-T

126474800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33648197-G-A

126475174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33647836-G-A

126475174-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33647836-G-T

126479209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33646726-C-T

126479234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33646703-C-T

126479341-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33646574-C-G

http://identifiers.org/hco/9/GRCh38#126480534-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33645822-C-A

126480534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33645822-C-T

126480686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33645681-G-A

126480698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33645655-C-T

126480710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33645643-C-T

126480711-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33645642-A-T

126480745-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33645608-G-T

126480777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33645583-G-A

126480777-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33645583-G-C

126480777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron variant
orthologous variants: 33645583-G-T

http://identifiers.org/hco/9/GRCh38#126480929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33645463-C-A

126481056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 33645341-G-A

126481056-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 33645341-G-C

126481056-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 33645341-G-T

http://identifiers.org/hco/9/GRCh38#126481066-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33645331-C-A

126481066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 33645331-C-T

http://identifiers.org/hco/9/GRCh38#126481159-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33645257-C-A

126481159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 33645257-C-T

126481194-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 33645219-T-G

http://identifiers.org/hco/9/GRCh38#126481197-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33645216-C-A

126481197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 33645216-C-T

126481208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 33645206-G-A

126481208-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 33645206-G-T

126481257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 33645154-G-A

126481257-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 33645154-G-T

http://identifiers.org/hco/9/GRCh38#126481262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33645149-C-A

126481262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 33645149-C-T

126481860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33644632-A-G

126481934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33644559-G-A

126481978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33644541-A-G

126482098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33644455-G-A

126482620-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33643932-A-T

126482842-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33643708-G-T

126483187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33643047-C-T

126483393-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33642894-T-A

126483476-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33642826-G-C

126483658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33642663-G-A

http://identifiers.org/hco/9/GRCh38#126483699-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33642623-C-A

126483814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33642512-C-T

126483881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33642460-G-A

126483881-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33642460-G-T

126484015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 33642336-G-A

126484173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33642200-G-A

126484173-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33642200-G-T

126484409-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33642131-A-T

126486205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33641602-G-A

126486323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33641507-A-G

http://identifiers.org/hco/9/GRCh38#126486419-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33641402-A-C

126486566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33641268-G-A

http://identifiers.org/hco/9/GRCh38#126486714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33641070-C-A

126486919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33640948-G-A

126486921-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33640946-G-T

126486935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33640930-G-A

126486964-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33640902-T-A

126487045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33640822-G-A

126487104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33640769-C-T

126489336-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33638492-C-G

126489346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33638484-G-A

126489659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33638193-T-C

126489826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33638092-C-T

126489848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33638067-T-C

126489910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33638029-C-T

126490127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33637847-T-C

126490302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33637714-A-G

126490413-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33637631-T-G

126490496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33637589-C-T

126490573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33637520-C-T

126490575-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33637518-T-G

126490652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33637443-T-C

126491275-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33636828-C-G

126491436-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33636671-T-A

http://identifiers.org/hco/9/GRCh38#126491452-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#33636656-A-C

126491452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33636656-A-G

126491453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33636655-G-A

126494338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33629561-G-A

126494487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33629427-A-G

126494520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33629398-A-G

126494520-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33629398-A-T

126494557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33629362-C-T

126498566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33627599-A-G

126499069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33627150-G-A

126499197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33627033-T-C

126499895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33626317-C-T

126499917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33626295-G-A

126500106-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33626131-G-T

http://identifiers.org/hco/9/GRCh38#126500170-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33626070-C-A

126500413-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33625891-T-A

http://identifiers.org/hco/9/GRCh38#126500422-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33625882-A-C

126500422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33625882-A-G

126500422-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33625882-A-T

126500502-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33625799-T-G

126500720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33625538-G-A

126500728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33625530-C-T

126501257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33624799-C-T

126503177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 33623541-T-C

http://identifiers.org/hco/9/GRCh38#126503192-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33623526-C-A

126503192-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 33623526-C-G

126503192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 33623526-C-T

126503249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 33623469-A-G

126503249-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 33623469-A-T

126503288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33623431-G-A

http://identifiers.org/hco/9/GRCh38#126503291-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33623428-C-A

126503313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33623396-G-A

126503313-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33623396-G-T

126503435-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33623284-T-A

126503435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33623284-T-C

126503435-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33623284-T-G

http://identifiers.org/hco/9/GRCh38#126503454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33623263-C-A

126503454-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33623263-C-G

126503511-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33623207-T-A

http://identifiers.org/hco/9/GRCh38#126503541-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33623186-C-A

126503541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33623186-C-T

126503565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33623154-G-A

126503571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33623148-C-T

126503687-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33623035-G-T

http://identifiers.org/hco/9/GRCh38#126503762-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33622961-A-C

http://identifiers.org/hco/9/GRCh38#126503860-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33622868-A-C

126503860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33622868-A-G

http://identifiers.org/hco/9/GRCh38#126503869-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33622859-C-A

126503869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33622859-C-T

126503892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33622831-C-T

126503912-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33622827-G-T

126503920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33622819-G-A

126503920-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33622819-G-T

http://identifiers.org/hco/9/GRCh38#126503956-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33622788-C-A

126503956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33622788-C-T

126504042-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33622692-G-T

http://identifiers.org/hco/9/GRCh38#126504073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33622661-C-A

126504073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33622661-C-T

126504118-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33622637-A-G

126504118-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33622637-A-T

http://identifiers.org/hco/9/GRCh38#126504127-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33622631-C-A

126504127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33622631-C-T

126504142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33622619-C-T

126504259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33622507-T-C

126504259-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33622507-T-G

126504302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33622475-A-G

126504316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33622461-A-G

126504327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33622448-G-A

126504327-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33622448-G-T

126504330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33622445-G-A

126504330-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33622445-G-T

126504347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33622438-A-G

126504490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33622324-T-C

126504540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33622285-G-A

126504540-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33622285-G-C

126504540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33622285-G-T

126504622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33622217-A-G

126504627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33622212-G-A

126504627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33622212-G-T

http://identifiers.org/hco/9/GRCh38#126504678-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33622158-C-A

126504678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33622158-C-T

126504827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33622024-T-C

126504929-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33621904-G-T

126504993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33621874-T-C

126505074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33621784-G-A

126505074-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33621784-G-C

126505074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33621784-G-T

126505094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33621764-C-T

126505138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33621724-T-C

126505146-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33621716-C-G

http://identifiers.org/hco/9/GRCh38#126505248-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33621634-C-A

126505299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33621587-A-G

126505428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33621499-A-G

126505429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33621498-G-T

126505446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33621481-A-G

http://identifiers.org/hco/9/GRCh38#126505451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33621478-C-A

126505451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33621478-C-T

126505452-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33621477-T-A

126505558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33621365-A-G

http://identifiers.org/hco/9/GRCh38#126505654-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33621282-C-A

126505654-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33621282-C-G

http://identifiers.org/hco/9/GRCh38#126505721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33621233-C-A

126505723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33621231-T-C

126505778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33621203-A-G

http://identifiers.org/hco/9/GRCh38#126505923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33621086-C-A

126505923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33621086-C-T

http://identifiers.org/hco/9/GRCh38#126505985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#33621019-C-A

126505985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33621019-C-T

126506198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33620750-G-A

126506198-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33620750-G-T

126506354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33620604-C-T

126506441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33620503-C-T

126506461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33620490-G-A

126506461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33620490-G-T

126506491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33620465-T-C

126506630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33620353-A-G

126506652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33620331-A-G