http://identifiers.org/hco/2/GRCh38#171999990-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#71283723-C-A

171999990-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 71283723-C-G

171999990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 71283723-C-T

http://identifiers.org/hco/2/GRCh38#172000154-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#71283843-C-A

172000595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71284170-G-A

172000600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71284175-G-A

172000642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71284217-G-A

172000642-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71284217-G-C

172000667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71284248-G-A

172000667-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71284248-G-C

172012195-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71296492-A-T

172012279-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71296578-C-G

172012321-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71296620-T-C

172013236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71297508-C-T

172013258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71297530-A-G

172013517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71297770-G-A

http://identifiers.org/hco/2/GRCh38#172017698-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#71300656-A-C

http://identifiers.org/hco/2/GRCh38#172017824-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#71300545-C-A

172018441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71300139-C-T

172018451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71300129-C-T

172021781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71304434-G-A

172021781-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71304434-G-T

http://identifiers.org/hco/2/GRCh38#172023447-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#71305787-A-C

172024253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71306338-C-T

172024450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71306517-A-G

172024764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71306826-G-A

172024821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71306866-G-A

172024881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71306926-C-T

172024893-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71306940-G-T

172024978-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71307018-G-C

172027821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71310019-C-T

172027920-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71310113-G-T

172028117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71310282-C-T

172028344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71310496-G-A

172030493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71312039-A-G

172030546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71312936-A-G

172030684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71313064-C-T

172031152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71313492-A-G

172031221-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71313553-A-G

172031830-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71314111-C-G

172031830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71314111-C-T

172031831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71314112-G-A

172031831-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71314112-G-C

172031849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71314130-A-G

172031903-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71314184-G-C

172032189-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71314474-C-G

172037964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71320166-T-C

172038204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71320387-G-A

172038212-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71320395-T-A

172038256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71320440-G-A

http://identifiers.org/hco/2/GRCh38#172042104-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#71320865-A-C

172045926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71323410-A-G

172046631-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71324073-A-T

172046780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71324214-C-T

172047383-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71324813-G-T

172047824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71325049-A-G

172047863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71325086-A-G

172047877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71325100-T-C

172048498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71325568-C-T

172049291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-C

172049325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-G

http://identifiers.org/hco/2/GRCh38#172049541-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#71326644-A-C

172049614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71326722-T-C

http://identifiers.org/hco/2/GRCh38#172049678-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#71326787-C-A

http://identifiers.org/hco/2/GRCh38#172050087-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#71327153-A-C

172050087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71327153-A-G

172050117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71327183-A-G

172050396-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71327471-T-A

172050396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71327471-T-C

http://identifiers.org/hco/2/GRCh38#172050406-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#71327481-A-C

172050406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71327481-A-G

172050617-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71327683-T-G

172050702-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71327767-T-G

172050777-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71327830-T-G

172050856-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71327940-C-G

http://identifiers.org/hco/2/GRCh38#172051037-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#71328120-C-A

172051037-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71328120-C-G

172051125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71328228-T-C

172051583-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71328919-T-A

172051583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71328919-T-C

172051603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71328939-G-A

172051671-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71329001-G-C

172051826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71329162-C-T

172052029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71329342-C-T

172052326-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71329649-T-G

172052910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71330232-T-C

172053133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71330449-A-G

172054969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71331922-T-C

172055087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71331824-G-A

172055099-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71331813-A-T

172055565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71332428-A-G

172055985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71332856-A-G

172056005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71332877-G-A

172056279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71333132-T-C

http://identifiers.org/hco/2/GRCh38#172056637-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#71333523-C-A

172056663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71333550-G-A

172056969-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71333846-A-T

172057001-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71333887-A-T

http://identifiers.org/hco/2/GRCh38#172057613-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#71334602-C-A

172057613-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71334602-C-G

172057752-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71334714-T-G

172058333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71335391-C-T

172060913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71336582-G-A

172060990-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71336627-C-G

http://identifiers.org/hco/2/GRCh38#172061016-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#71336653-A-C

172061016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71336653-A-G

172061193-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71336830-C-G

172061220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71336856-T-C

172061246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71336881-T-C

172061246-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71336881-T-G

172061325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71336958-A-G

172061329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71336962-T-C

172061354-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71336987-G-T

http://identifiers.org/hco/2/GRCh38#172061380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#71337012-C-A

172061380-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71337012-C-G

172061380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71337012-C-T

172061418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71337050-A-G

172061514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 71337145-C-T

http://identifiers.org/hco/2/GRCh38#172061628-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#71337259-A-C

172061674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71337314-T-C

172061867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71337489-G-A

172061867-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71337489-G-C

172061867-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71337489-G-T

172061951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71337574-G-A

172061951-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71337574-G-T

172061995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71337613-G-A

http://identifiers.org/hco/2/GRCh38#172062005-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#71337623-A-C

http://identifiers.org/hco/2/GRCh38#172062169-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#71337766-A-C

172062626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71338565-G-A

172062766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71339116-C-T

172062948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71339238-T-C

http://identifiers.org/hco/2/GRCh38#172063345-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#71339724-C-A

172063345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71339724-C-T

172063578-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71339951-T-G

172063731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 71340105-T-C

http://identifiers.org/hco/2/GRCh38#172064015-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#71340345-C-A

172064015-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71340345-C-G

172064015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71340345-C-T

172064030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71340360-A-G

172064140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71340464-T-C

172064249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71340570-T-C

172064689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71340831-A-G

172065240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71341380-G-A

172065315-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71341451-C-G

172065494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71341653-A-G

172065494-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71341653-A-T

172065568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71341724-A-G

172065643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71341795-C-T

172065956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71342099-A-G

172066046-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71342180-T-G

http://identifiers.org/hco/2/GRCh38#172066146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#71342352-C-A

172066146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71342352-C-T

http://identifiers.org/hco/2/GRCh38#172066148-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#71342354-C-A

172066148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71342354-C-T

172066150-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71342356-C-G

172066150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71342356-C-T

http://identifiers.org/hco/2/GRCh38#172066424-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#71342646-A-C

172066424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71342646-A-G

172066859-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71343078-G-T

172066868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71343087-G-A

172066868-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71343087-G-T

172066878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71343097-A-G

172066918-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71343142-T-A

172066928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71343154-G-A

172066928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71343154-G-T

172067083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71343332-A-G

172067413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71343658-C-T

172067415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71343660-A-G

172067531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71343761-G-A

172067710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71343928-A-G

172067733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71343950-T-C

172068054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71344259-G-A

172069841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71344976-G-A

172070329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71345446-T-C

172070346-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71345461-A-T

172070677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71345782-A-G

172070799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71345881-G-T

172071061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 71346135-A-G

172071079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71346153-T-C

172071081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71346155-C-T

172071114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71346187-A-G

172071114-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71346187-A-T

172073618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71348659-C-T

172073628-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71348669-G-C

172073904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71348949-A-G

172073908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71348957-T-C

172074022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71349069-T-C

172074075-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71349121-T-A

172074182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71349200-G-A

172074824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71349860-A-G

172075114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71350147-C-T

172075252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71350268-T-C

172075267-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71350283-G-C

172075381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71350375-T-C

172075930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71350889-G-A

172075962-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71350921-T-A

172076179-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71351141-T-A

172076430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71351566-C-T

172076805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71352005-A-G

172076955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71352162-C-T

172076964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71352174-A-G

172076964-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71352174-A-T

172077378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71352516-C-T

http://identifiers.org/hco/2/GRCh38#172077967-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#71353033-C-A

172077967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71353033-C-T

172078146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71353191-C-T

172078647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71353654-G-A

172078647-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71353654-G-T

172078786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71353749-C-T

172078939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71353874-G-A

172079042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71353991-C-T

172079043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71353992-G-A

172079162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71354097-T-C

172079274-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71354211-T-A

172079274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71354211-T-C

172080056-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71355011-A-T

172080317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71355216-C-T

172080475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 71355349-T-C

172080560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 71355402-G-A

172080560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 71355402-G-T

172080725-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 71355486-C-G

http://identifiers.org/hco/2/GRCh38#172080747-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#71355524-A-C

http://identifiers.org/hco/2/GRCh38#172080779-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#71355554-C-A

http://identifiers.org/hco/2/GRCh38#172080784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#71355559-C-A

http://identifiers.org/hco/2/GRCh38#172080965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#71355786-C-A

http://identifiers.org/hco/2/GRCh38#172081020-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#71355836-A-C

172081020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 71355836-A-G

172081020-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 71355836-A-T

172081036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 71355852-A-G

172081094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 71355903-C-T

http://identifiers.org/hco/2/GRCh38#172081118-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#71355920-C-A

172081118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 71355920-C-T

http://identifiers.org/hco/2/GRCh38#172081184-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#71355959-C-A

172081184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 71355959-C-T

172081207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 71355979-T-C

172081207-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 71355979-T-G

172081215-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 71355987-C-G

172081227-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 71355999-G-T

172081322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 71356075-G-A

172081322-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 71356075-G-C

172081322-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 71356075-G-T

172081387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 71356132-A-G

http://identifiers.org/hco/2/GRCh38#172081468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#71356215-C-A

172081553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 71356271-C-T

172081653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 71356367-C-T

http://identifiers.org/hco/2/GRCh38#172081680-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#71356380-C-A

172081685-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 71356385-G-T

172081696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 71356394-G-A

172081746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 71356442-T-C

172081826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 71356523-C-T

172081827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 71356524-G-A

172081903-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 71356598-G-T

172082076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 71356760-A-G

172082102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 71356786-G-A

172082102-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32583
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 71356786-G-T