155644489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28522008-G-A

155644489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28522008-G-T

155644507-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28522026-T-G

155644571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28522089-G-A

155644571-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28522089-G-T

155644589-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28522104-G-T

http://identifiers.org/hco/7/GRCh38#155644622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#28522132-C-A

155644622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28522132-C-T

155645323-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: intron_variant, undefined
orthologous variants: 28522584-G-C

155645323-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: intron_variant, undefined
orthologous variants: 28522584-G-T

155645341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: intron_variant, undefined
orthologous variants: 28522599-T-C

155645342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: intron_variant, undefined
orthologous variants: 28522600-A-G

155645675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: intron variant
orthologous variants: 28522886-A-G

155645813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: intron variant
orthologous variants: 28523011-A-G

155646015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: intron variant
orthologous variants: 28523211-C-T

155646056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: intron variant
orthologous variants: 28523254-A-G

http://identifiers.org/hco/7/GRCh38#155646430-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#28523617-C-A

155646439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: intron variant
orthologous variants: 28523626-C-T

155646824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: intron variant
orthologous variants: 28524591-G-A

155646843-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: intron variant
orthologous variants: 28524611-T-G

155647216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: intron variant
orthologous variants: 28524937-T-C

http://identifiers.org/hco/7/GRCh38#155647303-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#28525012-C-A

http://identifiers.org/hco/7/GRCh38#155647365-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#28525080-C-A

155647826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: intron variant
orthologous variants: 28525399-T-C

155647863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: intron variant
orthologous variants: 28525432-G-A

155664667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: intron variant
orthologous variants: 28535714-T-C

155664929-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: intron variant
orthologous variants: 28535924-G-T

155665089-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: intron variant
orthologous variants: 28536029-T-A

155665089-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: intron variant
orthologous variants: 28536029-T-G

155665103-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: intron variant
orthologous variants: 28536043-T-A

155665160-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: intron variant
orthologous variants: 28536094-G-T

155665343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: intron variant
orthologous variants: 28536271-A-G

155665474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: intron variant
orthologous variants: 28536392-T-C

155665517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: intron variant
orthologous variants: 28536428-C-T

155665568-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: intron variant
orthologous variants: 28536449-T-A

155665687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: intron variant
orthologous variants: 28536555-G-A

155671161-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: intron variant
orthologous variants: 28539342-C-G

155671226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: intron variant
orthologous variants: 28539400-A-G

155671451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: intron variant
orthologous variants: 28539566-C-T

155671901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: intron variant
orthologous variants: 28539996-T-C

http://identifiers.org/hco/7/GRCh38#155672031-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#28540124-C-A

155672096-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: intron variant
orthologous variants: 28540177-A-T

155672118-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: intron variant
orthologous variants: 28540414-T-G

155672242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: intron variant
orthologous variants: 28540539-T-C

155672390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: intron variant
orthologous variants: 28540661-G-T

155672831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: intron variant
orthologous variants: 28540791-A-G

155677685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28541035-C-T

http://identifiers.org/hco/7/GRCh38#155677687-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#28541037-A-C

155677687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28541037-A-G

155678043-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28541334-T-G

155678064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28541355-G-A

155678264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28541573-C-T

http://identifiers.org/hco/7/GRCh38#155678468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#28541824-C-A

155678468-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28541824-C-G

155678468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28541824-C-T

155678553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28541917-A-G

155678559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28541923-T-C

155678575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28541939-A-G

155678575-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28541939-A-T

155678764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28542130-G-A

155679769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28542643-A-G

http://identifiers.org/hco/7/GRCh38#155680336-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#28543800-A-C

155680336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28543800-A-G

155680475-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28543893-G-T

155680533-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28543944-T-G

155682725-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 28545656-G-C

155682959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28545872-C-T

155683251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28546109-G-T

155683299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28546148-C-T

155683305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28546154-C-T

155683444-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28546281-C-G

155683444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28546281-C-T

155684345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28546856-G-T

155684353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28546864-G-A

155684402-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28546917-T-G

155684718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28547204-C-T

155684869-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28547333-G-T

155684941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 28547401-A-G

155684941-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 28547401-A-T

http://identifiers.org/hco/7/GRCh38#155685147-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#28547605-C-A

155685147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28547605-C-T

155685206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28547657-G-A

155685241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28547749-G-A

155685263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28547777-T-C

http://identifiers.org/hco/7/GRCh38#155685887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#28548381-C-A

http://identifiers.org/hco/7/GRCh38#155685989-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#28548425-A-C

155686124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28548516-A-G

155686132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28548527-A-G

155699416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28556233-G-A

http://identifiers.org/hco/7/GRCh38#155700159-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#28556910-C-A

155700613-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28557362-G-T

155700657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28557407-G-A

155700657-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28557407-G-T

155700663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28557413-T-C

http://identifiers.org/hco/7/GRCh38#155700966-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#28557686-C-A

155700966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 28557686-C-T

155700979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 28557713-T-C

http://identifiers.org/hco/7/GRCh38#155700990-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#28557724-C-A

155700990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 28557724-C-T

155701185-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 28557902-T-A

155701185-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 28557902-T-G

155701186-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 28557912-T-G

155701236-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 28557967-G-T

155701409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 28558123-A-G

http://identifiers.org/hco/7/GRCh38#155701423-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#28558131-C-A

155703451-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28560069-T-G

http://identifiers.org/hco/7/GRCh38#155703453-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#28560071-A-C

155703890-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28560461-T-C

155703976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28560680-A-G

http://identifiers.org/hco/7/GRCh38#155703988-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#28560783-A-C

155704007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28560839-A-G

155704171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28560980-G-A

155704816-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28561555-C-G

155704816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28561555-C-T

155705001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28561712-C-T

155705369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28562074-G-A

155705394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28562098-T-C

http://identifiers.org/hco/7/GRCh38#155705401-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#28562105-A-C

155705401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28562105-A-G

155705500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28562199-A-G

155705635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28562301-A-G

155705686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28562359-C-T

155705688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28562361-A-G

155705733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28562428-C-T

http://identifiers.org/hco/7/GRCh38#155706005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#28562716-C-A

155706047-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28562763-T-A

155706070-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28562785-C-G

155706070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28562785-C-T

155706079-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28562806-G-C

155706761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28563181-G-A

155706761-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28563181-G-T

http://identifiers.org/hco/7/GRCh38#155706781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#28563201-C-A

155706781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28563201-C-T

155707026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 28563438-G-A

155707026-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 28563438-G-C

155707026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 28563438-G-T

155707085-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28563498-T-A

155707176-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28563581-G-C

155707176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28563581-G-T

155707195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28563599-G-A

155707195-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28563599-G-T

155707268-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28563672-T-A

155707269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28563673-A-G

155707294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 28563691-A-G

http://identifiers.org/hco/7/GRCh38#155707330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#28563714-C-A

155707621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28563950-A-G

155707621-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28563950-A-T

155707646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28563972-T-C

155708649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28564460-C-T

155708672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28564487-C-T

155710027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28565831-G-A

155710052-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28565857-T-A

155710294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28566075-G-A

155710333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28566117-G-A

155710360-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28566140-G-C

155710399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28566158-C-T

155710479-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28566206-C-G

155710750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28566451-C-T

155711158-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28566929-T-A

155711304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 28567081-G-A

155711304-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 28567081-G-C

155711304-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 28567081-G-T

155711340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 28567117-T-C

155715372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28570035-G-A

http://identifiers.org/hco/7/GRCh38#155715650-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#28570281-C-A

155716517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28571548-T-C

155716629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28571628-G-A

155716696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28571693-C-T

155717027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28571925-A-G

155717375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28572189-T-C

155717424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28572241-A-G

http://identifiers.org/hco/7/GRCh38#155717793-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#28572639-C-A

155718280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28573157-T-C

http://identifiers.org/hco/7/GRCh38#155718531-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#28573372-C-A

155718531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28573372-C-T

155718560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28573400-T-C

155718800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28573592-T-C

155719254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28573901-G-A

155719433-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28574035-G-C

155721019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28575410-T-C

155721110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28575488-T-C

155721525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28576250-A-G

155721553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28576265-C-T

155722998-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28578595-T-G

155723695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28579261-G-A

155725830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28580517-A-G

155726398-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28581065-G-T

155729924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28583379-A-G

155729957-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28583422-C-G

155730007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28583494-A-G

155730044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28583530-G-A

155730071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28583557-A-G

http://identifiers.org/hco/7/GRCh38#155730189-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#28583678-A-C

155732746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28586900-G-T

155733191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28587328-A-G

155733250-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28587363-A-T

155733447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28587503-T-C

http://identifiers.org/hco/7/GRCh38#155733464-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#28587520-C-A

155735065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28589086-C-T

155735112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28589152-T-C

155735353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28589306-G-A

155735426-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28589379-C-G

155735426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28589379-C-T

155736488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28590739-A-G

155736889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28591252-A-G

155736962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28591318-G-A

155737453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28591427-A-G

155737811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28591749-T-C

155737811-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28591749-T-G

155737945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28591879-A-G

155737999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28592597-C-T

155738020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28592611-C-T

155738127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 28592712-G-A

155738257-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 28592842-G-C

155738439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 28593026-G-A

155739532-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 28594141-T-A

155739532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 28594141-T-C

155739635-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 28594420-T-A

155739635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 28594420-T-C

155739732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 28594518-A-G

http://identifiers.org/hco/7/GRCh38#155739780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#28594572-C-A

155739780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 28594572-C-T

http://identifiers.org/hco/7/GRCh38#155739915-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#28594704-C-A

155739915-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 28594704-C-G

155739915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 28594704-C-T

155739941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 28594730-C-T

155739960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 28594749-A-G

155740029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28594818-A-G

155740029-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28594818-A-T

155740297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28594949-A-G

155741384-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 28595525-T-A

155741805-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28595869-C-G

155741805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28595869-C-T

155741944-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 28596007-C-G

155742038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, undefined
orthologous variants: 28596101-A-G

155742067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 28596130-T-C

155742079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 28596142-T-C

155742089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, undefined
orthologous variants: 28596152-G-A

http://identifiers.org/hco/7/GRCh38#155742158-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#28596217-A-C

155742158-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28596217-A-T

http://identifiers.org/hco/7/GRCh38#155742186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#28596245-C-A

155742186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28596245-C-T

155742331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28596277-G-A

155742494-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28596423-T-A

155743232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28596915-C-T

155743800-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28598017-C-G

155743800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28598017-C-T

http://identifiers.org/hco/7/GRCh38#155744846-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#28598902-C-A

155744846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28598902-C-T

155744912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28598954-G-A

155744912-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 28598954-G-T

155745020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 28599059-C-T

155745110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 28599149-G-A

155745110-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 28599149-G-C

155745135-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 28599179-C-G

155745135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 28599179-C-T

155745164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 28599254-A-G

155745278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 28599368-C-T

http://identifiers.org/hco/7/GRCh38#155745293-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#28599383-A-C

155745293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 28599383-A-G

155745488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 28599551-G-A

http://identifiers.org/hco/7/GRCh38#155745696-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#28599747-A-C

155746777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: intron variant
orthologous variants: 28600314-T-C

155747246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: intron variant
orthologous variants: 28600687-A-G

155747950-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: intron variant
orthologous variants: 28601490-A-T

155751057-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: intron variant
orthologous variants: 28604338-T-C

155751262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: intron variant
orthologous variants: 28604527-A-G

http://identifiers.org/hco/7/GRCh38#155751639-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#28604857-C-A

155751693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: intron variant
orthologous variants: 28604903-A-G

155752153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: intron variant
orthologous variants: 28605278-A-G

155754537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: intron variant
orthologous variants: 28608359-T-C

155754935-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: intron variant
orthologous variants: 28608770-T-A

155755924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: intron variant
orthologous variants: 28609727-C-T

155756044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: intron variant
orthologous variants: 28609840-T-C

155756082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: intron variant
orthologous variants: 28609864-C-T

155756083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: intron variant
orthologous variants: 28609865-G-A

155756250-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: intron variant
orthologous variants: 28610035-T-A

155756293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: intron variant
orthologous variants: 28610057-A-G

155763555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: intron variant
orthologous variants: 28613005-C-T

http://identifiers.org/hco/7/GRCh38#155763724-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#28613175-C-A

155763724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: intron variant
orthologous variants: 28613175-C-T

155763811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 5_prime_UTR_variant, splice_region_variant, synonymous_variant, undefined
orthologous variants: 28613252-G-A

155763919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 28613360-G-A

155763919-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 28613360-G-C

155763919-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 28613360-G-T

155764099-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: intron variant
orthologous variants: 28613524-G-T

155764289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: intron variant
orthologous variants: 28613644-G-A

http://identifiers.org/hco/7/GRCh38#155764969-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#28614148-A-C

155766348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: intron variant
orthologous variants: 28615450-T-C

155766439-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: intron variant
orthologous variants: 28615541-C-G

155766439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: intron variant
orthologous variants: 28615541-C-T

155766446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: intron variant
orthologous variants: 28615548-T-C

155766502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: synonymous variant
orthologous variants: 28615604-T-C

155766650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: missense variant
orthologous variants: 28615752-A-G

http://identifiers.org/hco/7/GRCh38#155766677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#28615780-C-A

155766781-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28615857-G-C

155766781-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28615857-G-T

155774501-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: intron variant
orthologous variants: 28618218-T-A

155774594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: missense variant
orthologous variants: 28618320-A-G

155774665-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: intron variant
orthologous variants: 28618391-T-G

155774681-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: intron variant
orthologous variants: 28618402-G-T

http://identifiers.org/hco/7/GRCh38#155774929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#28618507-C-A

155775097-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 28618668-G-C

155775332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3 prime UTR variant
orthologous variants: 28618894-A-G

155775577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3 prime UTR variant
orthologous variants: 28619140-A-G

155775614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3 prime UTR variant
orthologous variants: 28619177-G-A

http://identifiers.org/hco/7/GRCh38#155775688-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#28619239-A-C

155775688-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3 prime UTR variant
orthologous variants: 28619239-A-T

155775775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3 prime UTR variant
orthologous variants: 28619287-T-C

155775837-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3 prime UTR variant
orthologous variants: 28619351-T-G

http://identifiers.org/hco/7/GRCh38#155776090-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#28619551-C-A

155776130-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3 prime UTR variant
orthologous variants: 28619578-G-T

155776431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3 prime UTR variant
orthologous variants: 28619818-G-T

155776470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3 prime UTR variant
orthologous variants: 28619857-C-T

155776481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3 prime UTR variant
orthologous variants: 28619869-G-A

155776481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3 prime UTR variant
orthologous variants: 28619869-G-T

155776607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3 prime UTR variant
orthologous variants: 28619988-A-G

155776714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3 prime UTR variant
orthologous variants: 28620090-G-A

http://identifiers.org/hco/7/GRCh38#155776770-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#28620132-C-A

155777011-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3 prime UTR variant
orthologous variants: 28620308-T-G

155777065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3 prime UTR variant
orthologous variants: 28620360-C-T

155777155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3 prime UTR variant
orthologous variants: 28620434-C-T

155777192-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3 prime UTR variant
orthologous variants: 28620465-G-T

155777198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3 prime UTR variant
orthologous variants: 28620472-G-A

155777198-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3 prime UTR variant
orthologous variants: 28620472-G-T

http://identifiers.org/hco/7/GRCh38#155777572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#28620844-C-A

155777572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3 prime UTR variant
orthologous variants: 28620844-C-T

155778001-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3 prime UTR variant
orthologous variants: 28621262-C-G

155778027-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3 prime UTR variant
orthologous variants: 28621293-G-T

155778131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3 prime UTR variant
orthologous variants: 28621404-C-T

155778136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3 prime UTR variant
orthologous variants: 28621409-G-A

155778184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3 prime UTR variant
orthologous variants: 28621462-G-A

http://identifiers.org/hco/7/GRCh38#155778206-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#28621484-C-A

http://identifiers.org/hco/7/GRCh38#155778334-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#28621577-C-A

155778334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3 prime UTR variant
orthologous variants: 28621577-C-T

155778378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3 prime UTR variant
orthologous variants: 28621618-T-C

155778660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3 prime UTR variant
orthologous variants: 28621811-G-A

155778660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3 prime UTR variant
orthologous variants: 28621811-G-T

155778841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3 prime UTR variant
orthologous variants: 28621948-G-A

155778841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3 prime UTR variant
orthologous variants: 28621948-G-T

155778860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3 prime UTR variant
orthologous variants: 28621967-T-C

http://identifiers.org/hco/7/GRCh38#155778883-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#28621990-A-C

155778883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3 prime UTR variant
orthologous variants: 28621990-A-G

http://identifiers.org/hco/7/GRCh38#155779015-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#28622099-C-A

155779111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3 prime UTR variant
orthologous variants: 28622179-C-T

155779128-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3 prime UTR variant
orthologous variants: 28622196-G-C

155779242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3 prime UTR variant
orthologous variants: 28622244-G-A

155779312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3 prime UTR variant
orthologous variants: 28622297-T-C

155779312-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3 prime UTR variant
orthologous variants: 28622297-T-G

155780041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3 prime UTR variant
orthologous variants: 28622951-T-C

http://identifiers.org/hco/7/GRCh38#155780239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#28623126-C-A

155780239-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3 prime UTR variant
orthologous variants: 28623126-C-G

155780239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3 prime UTR variant
orthologous variants: 28623126-C-T

155780356-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3 prime UTR variant
orthologous variants: 28623232-A-T

155780377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3 prime UTR variant
orthologous variants: 28623252-T-C

155780380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3 prime UTR variant
orthologous variants: 28623255-C-T

155780389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3 prime UTR variant
orthologous variants: 28623264-A-G

155780407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3 prime UTR variant
orthologous variants: 28623279-A-G

http://identifiers.org/hco/7/GRCh38#155780409-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#28623281-C-A

155781158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3 prime UTR variant
orthologous variants: 28623935-G-A

155781158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3 prime UTR variant
orthologous variants: 28623935-G-T

155781485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27223
most severe consequence: 3 prime UTR variant
orthologous variants: 28624240-G-A