169694488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 69619973-G-A

169694488-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 69619973-G-C

169694488-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 69619973-G-T

169694494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 69619979-A-G

169694494-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 69619979-A-T

169694514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 69620003-G-A

169694514-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 69620003-G-T

http://identifiers.org/hco/2/GRCh38#169694515-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#69620004-C-A

169694515-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 69620004-C-G

169694515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 69620004-C-T

169694531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 69620024-G-A

169694531-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 69620024-G-T

169694537-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 69620030-C-G

169694537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 69620030-C-T

169694550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 69620043-G-A

169694550-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 69620043-G-C

169694550-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 69620043-G-T

169694585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 69620072-G-A

169694594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 69620081-G-A

169694594-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 69620081-G-T

169694609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 69620097-G-A

169694609-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 69620097-G-T

169694623-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_donor_variant, undefined
orthologous variants: 69620116-G-T

169694737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69620185-G-A

169694737-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69620185-G-T

169694741-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 69620189-G-C

169694741-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 69620189-G-T

169694796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69620241-G-A

169694796-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69620241-G-C

169694796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69620241-G-T

169695816-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69620902-A-T

169696102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69621140-G-A

169696111-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69621149-T-A

169696180-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69621217-T-A

169696180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69621217-T-C

169696340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69621406-A-G

http://identifiers.org/hco/2/GRCh38#169696981-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69622418-A-C

169697034-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69622440-G-T

169697052-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69622458-G-T

169697055-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69622461-G-C

169697055-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69622461-G-T

169697128-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69622523-G-C

169697161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69622555-G-T

169697164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69622558-C-T

169697172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69622566-C-T

http://identifiers.org/hco/2/GRCh38#169697976-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69624213-A-C

169697976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 69624213-A-G

169698986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69624945-A-G

169700910-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69625784-G-C

169700910-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69625784-G-T

169700980-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 69625854-T-G

169701046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 69625920-T-C

169701344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 69626218-C-T

169701701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69626575-G-A

169701792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69626660-G-A

169701792-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69626660-G-C

169701852-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69626706-T-A

169701924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69626779-C-T

169702031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69626882-C-T

169702155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69626999-G-A

169702155-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69626999-G-C

169702725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69628017-A-G

http://identifiers.org/hco/2/GRCh38#169702759-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69628049-C-A

169702759-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69628049-C-G

169720063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69646336-A-G

169720096-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69646366-G-T

http://identifiers.org/hco/2/GRCh38#169720159-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69646422-A-C

169720159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69646422-A-G

http://identifiers.org/hco/2/GRCh38#169720198-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69646475-C-A

169720340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69646642-G-A

169720635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69646972-C-T

169720642-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69646979-G-C

http://identifiers.org/hco/2/GRCh38#169720715-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69647049-A-C

169720715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69647049-A-G

169720715-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69647049-A-T

http://identifiers.org/hco/2/GRCh38#169720733-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69647067-C-A

169720733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69647067-C-T

169720757-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69647074-T-A

169720757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69647074-T-C

169723332-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69648982-T-G

169731046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69650419-T-C

169731243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69650571-T-C

169731528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69651296-C-T

169731530-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69651298-T-G

169732098-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69651816-G-T

169732140-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69651859-T-G

169732998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69652445-G-A

169733002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69652449-A-G

169733096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69652560-C-T

169733712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69653071-A-G

169733714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69653072-A-G

http://identifiers.org/hco/2/GRCh38#169733750-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#69653081-C-A

169733750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69653081-C-T

169733762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69653090-G-A

http://identifiers.org/hco/2/GRCh38#169733888-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69653130-C-A

169733888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69653130-C-T

http://identifiers.org/hco/2/GRCh38#169733953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69653189-C-A

169733953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69653189-C-T

169733992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69653229-G-A

169733992-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69653229-G-T

http://identifiers.org/hco/2/GRCh38#169734065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#69653311-C-A

169734065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69653311-C-T

169734118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69653359-C-T

169734124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69653365-T-C

169734124-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69653365-T-G

169734130-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69653369-G-T

169734153-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69653389-G-C

169734153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69653389-G-T

169734189-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69653407-G-T

169734306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69653514-G-A

169734408-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69653614-G-C

169734408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69653614-G-T

169734729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69653849-C-T

169734925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69654038-A-G

169735021-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 69654138-C-G

169735168-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 69654285-C-G

169735168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 69654285-C-T

169735296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 69654413-T-C

169735464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 69654581-G-A

169735992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 69655109-G-A

169736049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 69655166-A-G

169736130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 69655247-T-C

169736136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 69655253-A-G

169736357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69655495-A-G

169736371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69655509-A-G

169736371-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69655509-A-T

169736580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69656444-T-C

http://identifiers.org/hco/2/GRCh38#169736650-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69656516-A-C

169736650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69656516-A-G

169736669-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69656539-A-G

169736684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69656559-C-T

169736857-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69656735-G-T

169737226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69657098-A-G

169737394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69657178-G-A

169737521-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69657299-G-C

http://identifiers.org/hco/2/GRCh38#169737968-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69657651-A-C

169738315-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69657873-C-G

http://identifiers.org/hco/2/GRCh38#169738409-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69658078-A-C

http://identifiers.org/hco/2/GRCh38#169738817-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69658448-A-C

169738817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69658448-A-G

169738817-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69658448-A-T

http://identifiers.org/hco/2/GRCh38#169739119-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69658494-A-C

169739572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69658872-A-G

169739572-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69658872-A-T

169739686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69658995-T-C

169741217-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 69659038-G-C

169741217-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 69659038-G-T

http://identifiers.org/hco/2/GRCh38#169741218-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69659039-A-C

http://identifiers.org/hco/2/GRCh38#169741220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69659041-C-A

169741220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 69659041-C-T

http://identifiers.org/hco/2/GRCh38#169741222-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69659043-C-A

169741222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 69659043-C-T

169741223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 69659044-A-G

169741231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 69659052-T-C

169741263-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 69659081-T-G

169741318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 69659128-A-G

169741574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69659379-A-G

169741574-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69659379-A-T

http://identifiers.org/hco/2/GRCh38#169741611-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69659419-C-A

169741611-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69659419-C-G

169741649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69659480-A-G

169741649-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69659480-A-T

169742231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69660268-A-G

169742577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69660633-C-T

169742685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69660723-G-A

169743035-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69661882-T-G

http://identifiers.org/hco/2/GRCh38#169743300-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69662597-A-C

169743323-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69662620-G-C

169748837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69663420-C-T

169748890-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69663477-G-C

http://identifiers.org/hco/2/GRCh38#169749346-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69663949-A-C

http://identifiers.org/hco/2/GRCh38#169749353-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69663954-C-A

169749353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69663954-C-T

http://identifiers.org/hco/2/GRCh38#169749366-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69663967-C-A

169749385-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69663979-T-A

169749444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 69664041-G-A

http://identifiers.org/hco/2/GRCh38#169749528-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69664125-A-C

169749531-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 69664128-T-G

169749832-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 69664408-G-C

169749832-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 69664408-G-T

169749839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 69664415-A-G

169749839-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 69664415-A-T

169749854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 69664430-A-G

169750215-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 69664566-G-T

169750272-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 69664622-G-T

169750315-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 69664669-G-T

169750368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 69664688-G-A

169750387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 69664706-T-C

169750399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 69664718-C-T

http://identifiers.org/hco/2/GRCh38#169750429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69664747-C-A

169750429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 69664747-C-T

169750507-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 69664877-A-T

169750614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 69664978-T-C

169750726-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 69665092-G-T

http://identifiers.org/hco/2/GRCh38#169750948-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69665305-C-A

169751051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 69665398-T-C

169751052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 69665399-G-A

169751052-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 69665399-G-T

http://identifiers.org/hco/2/GRCh38#169751092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69665432-C-A

169751102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 69665440-T-C

169751102-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 69665440-T-G

http://identifiers.org/hco/2/GRCh38#169751104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69665441-C-A

169751104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 69665441-C-T

http://identifiers.org/hco/2/GRCh38#169751117-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69665454-C-A

169751117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 69665454-C-T

169751670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 69666164-G-A

169751670-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 69666164-G-T

169751672-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 69666167-G-T

169751806-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 69666278-A-T

169752009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron variant
orthologous variants: 69666467-A-G

169752294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron variant
orthologous variants: 69666731-A-G

169753295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron variant
orthologous variants: 69667220-A-G

169753414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron variant
orthologous variants: 69667334-A-G

169753417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron variant
orthologous variants: 69667337-G-A

169761271-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron variant
orthologous variants: 69670526-T-G

169761294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron variant
orthologous variants: 69670549-T-C

169761294-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron variant
orthologous variants: 69670549-T-G

169761299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron variant
orthologous variants: 69670554-A-G

169761404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron variant
orthologous variants: 69670643-G-A

169761436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron variant
orthologous variants: 69670676-C-T

169761503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, undefined
orthologous variants: 69670738-C-T

http://identifiers.org/hco/2/GRCh38#169761615-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#69670825-A-C

169761693-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron variant
orthologous variants: 69670904-C-G

169761794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, undefined
orthologous variants: 69671005-T-C

169761925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron_variant, undefined
orthologous variants: 69671139-G-A

169766895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron variant
orthologous variants: 69674226-G-A

169770972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron variant
orthologous variants: 69674484-G-A

169770972-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron variant
orthologous variants: 69674484-G-T

http://identifiers.org/hco/2/GRCh38#169771025-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69674528-A-C

169771235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron variant
orthologous variants: 69674716-A-G

169775476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron variant
orthologous variants: 69677158-C-T

http://identifiers.org/hco/2/GRCh38#169775930-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69678619-A-C

169776142-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron variant
orthologous variants: 69678835-T-A

169776331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron variant
orthologous variants: 69679046-G-A

169776331-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron variant
orthologous variants: 69679046-G-T

169776376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron variant
orthologous variants: 69679255-T-C

169776427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: intron variant
orthologous variants: 69679308-A-G

http://identifiers.org/hco/2/GRCh38#169776442-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69679323-C-A

169776442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 69679323-C-T

169776445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: synonymous variant
orthologous variants: 69679326-G-T

http://identifiers.org/hco/2/GRCh38#169776458-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69679341-A-C

169776458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: missense variant
orthologous variants: 69679341-A-G

169776488-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: 3 prime UTR variant
orthologous variants: 69679382-G-C

http://identifiers.org/hco/2/GRCh38#169776597-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#69679559-C-A

169776607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: 3 prime UTR variant
orthologous variants: 69679569-G-A

169776607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: 3 prime UTR variant
orthologous variants: 69679569-G-T

169776762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: 3 prime UTR variant
orthologous variants: 69679696-G-A

169776762-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: 3 prime UTR variant
orthologous variants: 69679696-G-T

169776798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: 3 prime UTR variant
orthologous variants: 69679711-T-C

169776805-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: 3 prime UTR variant
orthologous variants: 69679718-T-A

169776805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: 3 prime UTR variant
orthologous variants: 69679718-T-C

169776809-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: 3 prime UTR variant
orthologous variants: 69679722-T-G

169776815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: 3 prime UTR variant
orthologous variants: 69679728-G-A

169776815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: 3 prime UTR variant
orthologous variants: 69679728-G-T

169776917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27506
most severe consequence: 3 prime UTR variant
orthologous variants: 69679804-T-C