17027245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 40761065-G-A

17027245-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 40761065-G-C

17027245-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 40761065-G-T

http://identifiers.org/hco/8/GRCh38#17027253-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#40761073-C-A

17027253-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 40761073-C-G

17027253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 40761073-C-T

http://identifiers.org/hco/8/GRCh38#17027298-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#40761110-C-A

17027298-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 40761110-C-G

17027298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 40761110-C-T

http://identifiers.org/hco/8/GRCh38#17027300-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#40761112-C-A

17027300-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 40761112-C-G

17027300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 40761112-C-T

17027334-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 40761146-T-A

17027334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 40761146-T-C

http://identifiers.org/hco/8/GRCh38#17027498-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#40761307-C-A

17027498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 40761307-C-T

17027520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 40761329-G-A

17027520-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 40761329-G-C

http://identifiers.org/hco/8/GRCh38#17027612-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#40761403-C-A

17027612-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 40761403-C-G

17027612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 40761403-C-T

17027660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 40761451-G-A

17027660-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 40761451-G-C

17027660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 40761451-G-T

17027692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40761483-G-A

17027692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40761483-G-T

http://identifiers.org/hco/8/GRCh38#17027703-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#40761503-C-A

17027703-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40761503-C-G

17027703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40761503-C-T

17027715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40761520-G-A

17027715-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40761520-G-C

17027715-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40761520-G-T

http://identifiers.org/hco/8/GRCh38#17027731-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#40761575-A-C

17027731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40761575-A-G

http://identifiers.org/hco/8/GRCh38#17027734-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#40761578-C-A

17027734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40761578-C-T

17027769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40761614-A-G

17027797-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40761640-C-G

17028061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40761879-A-G

17028068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40761886-T-C

17028069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40761887-C-T

17028078-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40761894-G-C

17028110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40761917-T-C

17028247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40761993-C-T

http://identifiers.org/hco/8/GRCh38#17028640-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#40762396-C-A

17028656-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40762422-G-C

17028683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 40762449-G-A

17028752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40762523-A-G

17028752-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40762523-A-T

17028853-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40762621-T-G

17029000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40762767-A-G

17029115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40762793-G-A

17029604-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40763088-T-G

17029612-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40763095-T-A

17029762-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40763262-G-T

17029819-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40763303-T-G

17029872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40763344-C-T

17039835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40764082-A-G

17040509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40765681-T-C

17040677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40765837-G-A

17041551-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40767531-C-G

http://identifiers.org/hco/8/GRCh38#17041617-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#40767589-C-A

17041617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40767589-C-T

17041653-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40767626-G-T

17041676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40767646-T-C

17041756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40767712-G-A

17041917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40767888-C-T

17041932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40767905-A-G

17041940-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40767913-G-C

17041981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40767991-G-A

http://identifiers.org/hco/8/GRCh38#17042048-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#40768059-A-C

17042090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40768101-C-T

17042116-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40768127-T-C

17042271-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40768263-C-G

17047964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40769534-T-C

17048138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40769723-C-T

17052069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40778219-C-T

17052881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40778843-T-C

17053219-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40779166-T-G

17053499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40779444-C-T

17053763-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40780254-C-G

17053966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40780435-T-C

17053969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40780438-A-G

17054084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40780549-T-C

http://identifiers.org/hco/8/GRCh38#17054246-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#40780944-A-C

17054508-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40781107-T-A

17054658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40781266-A-G

17054692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40781298-G-A

17054692-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40781298-G-C

17056001-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40784131-C-G

17056194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40784278-G-A

17056376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40784423-A-G

17056433-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40784472-C-G

http://identifiers.org/hco/8/GRCh38#17058479-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#40785572-C-A

17059140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40786263-T-C

17064063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40788830-T-C

17064233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 40789000-C-T

17064252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40789019-G-A

17064252-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40789019-G-C

17064318-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40789210-T-G

17064322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40789214-T-C

http://identifiers.org/hco/8/GRCh38#17064378-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#40789288-A-C

17064378-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40789288-A-T

17064750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40789825-G-T

17064830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40789904-A-G

17064851-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40789928-A-T

17064867-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40789941-A-T

17064937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40790006-A-G

17064950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40790019-A-G

17065352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40790784-C-T

17065606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40791027-T-C

17065769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40791187-T-C

17065859-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40791238-G-C

17067807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40791640-G-A

17067887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40791709-C-T

17068057-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40791892-T-A

17068199-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40792064-A-T

17068251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40792124-A-G

17068358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40792231-C-T

17068659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40792466-A-G

17068772-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40792597-G-C

17068772-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40792597-G-T

17068895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40792680-T-C

17068930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40792714-T-C

17068993-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40792765-C-G

17069026-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40792798-G-C

http://identifiers.org/hco/8/GRCh38#17069083-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#40792827-A-C

17069083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40792827-A-G

17069357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40793025-A-G

17069480-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40793146-T-G

17069568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40793227-A-G

17072504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40797706-A-G

17072666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40797856-A-G

17072865-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40798044-T-A

17074235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40798480-A-G

17074693-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40798844-T-A

http://identifiers.org/hco/8/GRCh38#17074804-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#40798947-A-C

17074919-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40799079-T-A

17074920-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40799080-G-T

17074923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40799083-C-T

17074935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40799095-G-A

17075021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40799182-G-A

17075420-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40799492-A-T

17075485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40799555-A-G

17075770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40799771-G-A

17076004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40799943-T-C

17076397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40800029-A-G

17076426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40800059-G-A

17076481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40800115-G-T

17076501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40800134-G-A

17076627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40800248-C-T

http://identifiers.org/hco/8/GRCh38#17076972-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#40800751-A-C

17077413-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40801619-G-C

17077475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40801660-G-A

17077476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40801661-A-G

17077535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40801720-A-G

17077535-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40801720-A-T

17077657-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40801851-G-T

17077693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40801886-A-G

17077904-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40802114-T-A

17077904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40802114-T-C

17077982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40802186-A-G

17077984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40802188-A-G

17078072-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40802276-T-A

17078545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40802660-A-G

17078580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40802695-A-G

17078633-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40802719-A-G

17078633-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40802719-A-T

17078954-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40802998-A-T

17080210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40803787-C-T

17080302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40803868-A-G

17080434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40803991-A-G

17080624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40804079-T-C

17080624-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40804079-T-G

17080687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40804142-T-C

17080687-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40804142-T-G

17080825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40804275-A-G

17080932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40804378-G-A

17080967-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40804409-G-T

17080983-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40804424-T-A

17080983-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40804424-T-G

17081122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40804535-C-T

17081615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40804974-T-C

17081739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 40805123-A-G

17081739-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 40805123-A-T

17081775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 40805159-G-A

17081775-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 40805159-G-T

http://identifiers.org/hco/8/GRCh38#17081836-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#40805216-A-C

17081836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40805216-A-G

17081877-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40805257-A-T

17081882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40805262-T-C

17081945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40805322-A-G

17081952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40805329-T-C

http://identifiers.org/hco/8/GRCh38#17082007-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#40805373-C-A

17082007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40805373-C-T

17082076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40805437-A-G

17082296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40805646-C-T

17082299-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40805649-C-G

17082299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40805649-C-T

17082427-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40805743-C-G

17082646-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40805961-A-T

17084334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40806421-A-G

17084364-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40806449-T-G

17084370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40806455-A-G

17084384-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40806468-T-G

http://identifiers.org/hco/8/GRCh38#17084499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#40806557-C-A

17084535-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40806594-C-G

17084565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40806621-C-T

17085033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40807098-C-T

17085069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40807130-A-G

17085084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40807147-A-G

17085084-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40807147-A-T

17085109-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40807172-T-A

17085109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40807172-T-C

http://identifiers.org/hco/8/GRCh38#17085344-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#40807452-A-C

17085344-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40807452-A-G

17085344-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40807452-A-T

http://identifiers.org/hco/8/GRCh38#17085429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#40807505-C-A

17085429-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40807505-C-G

17085429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40807505-C-T

17085707-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40807661-T-A

17086075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40807971-G-A

17086075-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40807971-G-C

17086794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40809762-A-G

17086864-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40809819-G-C

17086864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40809819-G-T

17087730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40810654-A-G

17087777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40810701-G-T

17087845-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40810764-T-A

17087845-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40810764-T-G

17088910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40811046-G-A

17088910-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40811046-G-C

http://identifiers.org/hco/8/GRCh38#17088938-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#40811073-A-C

17088938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40811073-A-G

17089098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40811203-A-G

17089193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40811292-T-C

17089249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40811328-T-C

17089355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40811431-A-G

17089595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40811614-A-G

17090226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40812139-G-A

17090226-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40812139-G-C

17090244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40812160-A-G

17090546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 40812451-C-T

17090719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40812618-G-A

17090719-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40812618-G-T

17090819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40812708-A-G

17090944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40812861-C-T

17091128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40813001-T-C

17091209-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40813069-T-G

17091253-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40813089-G-C

17091253-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40813089-G-T

17091624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 40813371-G-A

17091644-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 40813390-C-G

17091655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 40813401-G-A

17091662-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40813408-T-G

17091836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 40813560-C-T

17092952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40814032-A-G

17093198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40814242-A-G

http://identifiers.org/hco/8/GRCh38#17093306-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#40814360-A-C

http://identifiers.org/hco/8/GRCh38#17093358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#40814412-C-A

17093358-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40814412-C-G

17093705-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40814770-C-G

17093879-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40814926-T-G

17096148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40817284-C-T

17096187-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40817322-G-T

http://identifiers.org/hco/8/GRCh38#17096196-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#40817331-A-C

17096199-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40817334-G-T

17096200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40817335-C-T

17096210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40817345-G-T

17096298-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 40817418-C-G

17096504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40817616-G-A

17096538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40817651-C-T

17096772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40817758-A-G

17096877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40817775-A-G

17097132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40817908-C-T

17097133-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40817909-A-T

17097177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40817952-A-G

17097227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40817996-A-G

17097719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40818515-T-C

17097883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40818633-G-A

17098321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40819059-A-G

17098357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40819082-A-G

17098395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40819129-A-G

17098441-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40819173-T-C

17098441-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40819173-T-G

http://identifiers.org/hco/8/GRCh38#17098449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#40819181-C-A

17098563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40819295-A-G

17098563-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40819295-A-T

17098570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40819302-A-G

17098572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40819304-A-G

17098574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40819306-G-A

17098574-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40819306-G-T

17102424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40819920-G-A

17102424-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40819920-G-T

17102468-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40819972-G-C

17102474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40819978-G-A

17102720-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40820214-T-G

17102777-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40820266-A-T

17102840-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40820330-T-G

17102871-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40820360-A-T

17103142-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40820828-T-G

17103300-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40820964-T-C

17103461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40821093-G-T

17103541-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40821158-A-T

http://identifiers.org/hco/8/GRCh38#17103622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#40821214-C-A

17103624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40821216-A-G

17103634-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40821226-A-T

17103926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40827923-G-A

17103963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40827957-C-T

17104045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40828019-A-G

17104117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40828086-T-C

17104240-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40828208-T-G

17104262-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40828231-A-T

17104287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40828471-C-T

17104298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40828480-T-C

17104319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40828498-T-C

17104537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40828717-A-G

17104537-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40828717-A-T

http://identifiers.org/hco/8/GRCh38#17104543-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#40828723-A-C

17104543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40828723-A-G

17104543-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40828723-A-T

17104990-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40828840-G-T

17105011-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40828845-A-T

17105119-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40828946-G-T

17105139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40828957-A-G

17105144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40828962-G-A

17105211-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40829023-G-T

http://identifiers.org/hco/8/GRCh38#17105363-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#40829110-C-A

17105363-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40829110-C-G

17105363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40829110-C-T

17105422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 40829146-T-C

17105512-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 40829236-T-G

17105593-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40829317-T-A

17105593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40829317-T-C

http://identifiers.org/hco/8/GRCh38#17105635-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#40829358-C-A

17105635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40829358-C-T

17105670-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40829408-G-C

17105670-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40829408-G-T

17105819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40829501-A-G

17105820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40829502-A-G

17105904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40829591-A-G

17105950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40829637-T-C

17106229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40829904-A-G

17106292-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40829967-T-A

http://identifiers.org/hco/8/GRCh38#17106322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#40829997-C-A

17106534-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40830190-G-T

17106548-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40830204-T-C

17106576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40830218-G-A

17106576-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40830218-G-T

http://identifiers.org/hco/8/GRCh38#17107066-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#40830642-C-A

17107142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40830709-G-A

17107142-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40830709-G-C

17107313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40830870-A-G

17107353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40830911-G-A

17107357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40830915-A-G

17107360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40830918-C-T

17107377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40830935-G-A

17107435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40830993-G-A

17107500-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40831057-G-C

17107500-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40831057-G-T

17107518-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40831078-G-C

17107526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40831086-G-A

17107526-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40831086-G-T

http://identifiers.org/hco/8/GRCh38#17113368-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#40831311-C-A

17113368-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40831311-C-G

17113368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40831311-C-T

17113494-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40831420-C-G

17113828-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40831694-T-G

17113963-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40831749-T-A

17113963-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40831749-T-G

17113972-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40831756-G-T

17113987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40831771-A-G

http://identifiers.org/hco/8/GRCh38#17114035-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#40831817-C-A

17114035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40831817-C-T

http://identifiers.org/hco/8/GRCh38#17114101-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#40831881-A-C

17114101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 40831881-A-G

17114212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40831992-A-G

17114243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40832031-T-C

http://identifiers.org/hco/8/GRCh38#17114271-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#40832059-A-C

17114271-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40832059-A-T

http://identifiers.org/hco/8/GRCh38#17114325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#40832114-C-A

17114325-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40832114-C-G

17114358-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40832180-G-C

17114367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40832189-C-T

17114406-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40832247-G-C

17114525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40832328-A-G

17114540-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40832341-A-T

17114634-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40832428-C-G

17115394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40832906-G-A

17115498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40833013-T-C

17115520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40833032-C-T

17115736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40833187-A-G

17116083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40833426-G-A

17116083-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40833426-G-T

17116327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40833606-T-C

17116331-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40833610-T-A

17116342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40833621-T-C

17116377-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40833648-C-G

17116377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40833648-C-T

17116427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40833697-T-C

17116567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 40833837-A-G

17116724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40833971-A-G

17116724-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40833971-A-T

17116725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40833972-A-G

17116736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40833988-T-C

17116796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40834046-T-C

17116860-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40834109-T-A

17116926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40834175-G-A

http://identifiers.org/hco/8/GRCh38#17117480-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#40834358-A-C

17117480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40834358-A-G

17118155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40834639-A-G

17118409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40834888-G-T

17118428-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40834907-T-A

17118459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40834930-G-A

17118588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40835049-G-A

17118588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40835049-G-T

17118593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40835054-T-C

http://identifiers.org/hco/8/GRCh38#17118603-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#40835064-C-A

17118794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40835237-G-A

17118887-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40835431-T-A

17118921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40835649-G-A

17118983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40835725-G-A

17118989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40835730-T-C

17119056-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40835798-A-T

17119358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40836305-C-T

17119374-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40836321-T-A

17119376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40836323-C-T

17119792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40836971-A-G

17119897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40837064-A-G

17119991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40837144-T-C

17120054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40837206-T-C

17120562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40837954-A-G

17120574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40837966-G-A

17120672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40838053-C-T

17120702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40838071-A-G

17120717-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40838086-C-G

17120753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40838123-A-G

http://identifiers.org/hco/8/GRCh38#17120868-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#40838239-A-C

17121073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40838416-T-C

17121116-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40838462-T-C

17121194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40838517-A-G

17121237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40838544-G-A

17121329-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40838647-T-G

17121585-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40839142-G-T

17121608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40839165-C-T

17121680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40839229-C-T

http://identifiers.org/hco/8/GRCh38#17121823-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#40839354-C-A

17121898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40839425-C-T

17122006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40839503-T-C

17122033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40839530-G-A

17122051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40839556-G-T

17122082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40839588-T-C

17122126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40839659-A-G

17122127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40839660-T-C

17122223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40839803-T-C

17122283-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40839867-A-T

17122308-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40839890-T-G

17122336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40839916-T-C

17122350-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40839930-T-G

17122351-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40839931-T-G

17123372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40840505-G-A

17123415-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40840555-G-C

17123658-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40840770-T-A