http://identifiers.org/hco/5/GRCh38#180601588-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49543489-A-C

180601588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3 prime UTR variant
orthologous variants: 49543489-A-G

180601633-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3 prime UTR variant
orthologous variants: 49543441-G-T

http://identifiers.org/hco/5/GRCh38#180601708-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49543327-A-C

180601708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3 prime UTR variant
orthologous variants: 49543327-A-G

http://identifiers.org/hco/5/GRCh38#180601712-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49543321-A-C

180601712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3 prime UTR variant
orthologous variants: 49543321-A-G

http://identifiers.org/hco/5/GRCh38#180601753-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49543275-A-C

180601753-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3 prime UTR variant
orthologous variants: 49543275-A-T

180601767-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3 prime UTR variant
orthologous variants: 49543261-C-G

180601767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3 prime UTR variant
orthologous variants: 49543261-C-T

180601768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3 prime UTR variant
orthologous variants: 49543260-G-A

180601768-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3 prime UTR variant
orthologous variants: 49543260-G-T

180601828-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3 prime UTR variant
orthologous variants: 49543197-G-T

180601844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3 prime UTR variant
orthologous variants: 49543191-A-G

180601844-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3 prime UTR variant
orthologous variants: 49543191-A-T

180601909-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3 prime UTR variant
orthologous variants: 49543135-T-G

180601930-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3 prime UTR variant
orthologous variants: 49543114-T-A

180601930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3 prime UTR variant
orthologous variants: 49543114-T-C

http://identifiers.org/hco/5/GRCh38#180601931-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49543113-C-A

180601931-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3 prime UTR variant
orthologous variants: 49543113-C-G

180601931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3 prime UTR variant
orthologous variants: 49543113-C-T

180601939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3 prime UTR variant
orthologous variants: 49543105-G-A

180601939-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3 prime UTR variant
orthologous variants: 49543105-G-T

180601969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3 prime UTR variant
orthologous variants: 49543085-T-C

180601973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3 prime UTR variant
orthologous variants: 49543081-G-A

180601973-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3 prime UTR variant
orthologous variants: 49543081-G-T

180601980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3 prime UTR variant
orthologous variants: 49543062-T-C

180601987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3 prime UTR variant
orthologous variants: 49543055-G-A

180601987-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3 prime UTR variant
orthologous variants: 49543055-G-T

180601994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3 prime UTR variant
orthologous variants: 49543048-G-A

180601994-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3 prime UTR variant
orthologous variants: 49543048-G-T

http://identifiers.org/hco/5/GRCh38#180602042-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49543030-C-A

180602091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3 prime UTR variant
orthologous variants: 49542996-G-A

180602106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3 prime UTR variant
orthologous variants: 49542981-G-A

180602106-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3 prime UTR variant
orthologous variants: 49542981-G-T

http://identifiers.org/hco/5/GRCh38#180602129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49542957-C-A

180602289-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3 prime UTR variant
orthologous variants: 49542840-A-G

http://identifiers.org/hco/5/GRCh38#180602300-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49542813-C-A

180602300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3 prime UTR variant
orthologous variants: 49542813-C-T

180602339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3 prime UTR variant
orthologous variants: 49542783-G-A

180602339-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3 prime UTR variant
orthologous variants: 49542783-G-T

180602387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3 prime UTR variant
orthologous variants: 49542714-T-C

180602412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3 prime UTR variant
orthologous variants: 49542684-A-G

180602413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3 prime UTR variant
orthologous variants: 49542683-T-C

180602425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3 prime UTR variant
orthologous variants: 49542677-A-G

180602452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3 prime UTR variant
orthologous variants: 49542647-T-C

180602453-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3 prime UTR variant
orthologous variants: 49542646-G-T

180602483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3 prime UTR variant
orthologous variants: 49542615-T-C

180602500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3 prime UTR variant
orthologous variants: 49542607-T-C

180602500-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3 prime UTR variant
orthologous variants: 49542607-T-G

180602511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3 prime UTR variant
orthologous variants: 49542596-A-G

180602539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3 prime UTR variant
orthologous variants: 49542536-A-G

http://identifiers.org/hco/5/GRCh38#180602604-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49542483-C-A

180602604-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3 prime UTR variant
orthologous variants: 49542483-C-G

180602664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3 prime UTR variant
orthologous variants: 49542420-G-T

180602748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3 prime UTR variant
orthologous variants: 49542337-G-A

180602765-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3 prime UTR variant
orthologous variants: 49542324-G-T

180602814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3 prime UTR variant
orthologous variants: 49542268-A-G

http://identifiers.org/hco/5/GRCh38#180602847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49542243-C-A

180602847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3 prime UTR variant
orthologous variants: 49542243-C-T

http://identifiers.org/hco/5/GRCh38#180602851-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49542239-C-A

180602851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3 prime UTR variant
orthologous variants: 49542239-C-T

180602917-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3 prime UTR variant
orthologous variants: 49542173-C-G

180602917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3 prime UTR variant
orthologous variants: 49542173-C-T

http://identifiers.org/hco/5/GRCh38#180603079-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49542013-C-A

180603096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 49541998-A-G

http://identifiers.org/hco/5/GRCh38#180603159-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49541941-C-A

180603159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 49541941-C-T

180603163-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 49541937-C-G

180603163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 49541937-C-T

180603208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 49541892-G-A

180603208-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 49541892-G-T

180603431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49541669-C-T

180603442-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49541658-G-C

180603442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49541658-G-T

180606143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 49541386-C-T

180606206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 49541329-G-A

180606275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49541260-A-G

180606298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49541237-C-T

http://identifiers.org/hco/5/GRCh38#180608837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49538990-C-A

180608837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49538990-C-T

180608889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49538937-A-G

http://identifiers.org/hco/5/GRCh38#180608926-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49538907-A-C

180608926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49538907-A-G

180609242-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49538577-G-T

180609582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49538425-G-A

180609582-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49538425-G-T

180609821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49536926-C-T

180609830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49536917-T-C

180609877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49536866-C-T

180609888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49536855-C-T

180610040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49536701-C-T

180610042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49536699-G-A

180610042-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49536699-G-C

180610054-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49536687-G-C

180610090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49536645-A-G

180610098-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49536637-T-A

180610098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49536637-T-C

http://identifiers.org/hco/5/GRCh38#180610470-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49536231-C-A

180610486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49536212-G-A

180610486-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49536212-G-C

180610536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49536166-G-A

http://identifiers.org/hco/5/GRCh38#180610579-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49536122-A-C

180610580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49536121-G-A

180610629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49536073-G-A

180610629-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49536073-G-C

180610651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49536050-C-T

180610734-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49535970-C-G

http://identifiers.org/hco/5/GRCh38#180610973-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49535714-C-A

180610973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49535714-C-T

180611253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49535337-G-A

180611253-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49535337-G-C

180611253-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49535337-G-T

180611268-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 49535328-T-A

180611268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 49535328-T-C

180611436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 49535152-G-A

180611461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 49535127-T-C

180611463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 49535125-C-T

180611495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 49535093-G-A

180611495-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 49535093-G-C

180611527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 49535069-C-T

http://identifiers.org/hco/5/GRCh38#180611640-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49535051-C-A

180611640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49535051-C-T

180611670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49535022-T-C

180611670-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49535022-T-G

180611693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49534999-T-C

180611708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49534984-G-A

180611783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49534907-G-A

180611788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49534902-G-A

180611788-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49534902-G-C

180611788-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49534902-G-T

180611806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49534884-G-A

180611810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49534880-C-T

180611845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49534845-T-C

180611845-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49534845-T-G

180611889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49534812-G-A

180611889-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49534812-G-C

http://identifiers.org/hco/5/GRCh38#180612095-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49534755-C-A

180612095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49534755-C-T

180612212-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49534656-G-T

180612225-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49534643-G-T

180612235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49534632-G-A

180612243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49534624-T-C

180612267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49534600-G-A

180612267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49534600-G-T

http://identifiers.org/hco/5/GRCh38#180612287-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49534580-C-A

180612287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49534580-C-T

180612346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49534532-G-A

180612346-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49534532-G-T

180612348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49534525-G-A

180612348-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49534525-G-C

180612370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49534499-G-A

180612370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49534499-G-T

180612378-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49534491-A-T

180612431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49534438-G-A

180612431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49534438-G-T

180612466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49534405-G-A

180612466-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49534405-G-T

180612497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49534374-G-A

180612631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 49534240-G-A

180612631-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 49534240-G-T

180612639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 49534232-G-A

180612639-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 49534232-G-T

180613035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 49533121-G-A

http://identifiers.org/hco/5/GRCh38#180613189-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49532977-C-A

180613192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49532974-T-C

180613917-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49531255-G-T

http://identifiers.org/hco/5/GRCh38#180613922-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49531250-C-A

180613953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49531223-A-G

180613953-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49531223-A-T

180614000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49531193-G-A

180614000-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49531193-G-T

180614015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49531178-T-C

180614015-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49531178-T-G

180614037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49531152-T-C

180614040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49531149-C-T

http://identifiers.org/hco/5/GRCh38#180614041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49531148-C-A

180614041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49531148-C-T

180614118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 49531068-T-C

180616284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49529286-C-T

180616339-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49529237-T-A

180616339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49529237-T-C

180616626-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49528957-T-A

http://identifiers.org/hco/5/GRCh38#180616791-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49528816-A-C

http://identifiers.org/hco/5/GRCh38#180616857-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49528753-A-C

180616887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49528716-G-A

180616887-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49528716-G-C

180616904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 49528701-C-T

180617123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49528481-T-C

180617146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49528464-C-T

180618611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49528353-G-A

180618621-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49528335-T-A

180618646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49528310-G-A

180618646-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49528310-G-C

http://identifiers.org/hco/5/GRCh38#180618670-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49528287-C-A

180618670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49528287-C-T

180618683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49528272-G-A

180618683-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49528272-G-C

180618683-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49528272-G-T

180618695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49528260-A-G

180618695-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49528260-A-T

http://identifiers.org/hco/5/GRCh38#180618707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49528248-C-A

180618707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49528248-C-T

180618735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49528208-A-G

180618768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: 49528179-A-G

180618907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 49528040-T-C

180618907-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 49528040-T-G

180618922-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_acceptor_variant, undefined
orthologous variants: 49528025-T-A

http://identifiers.org/hco/5/GRCh38#180618930-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#49528017-C-A

180618930-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 49528017-C-G

180618930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 49528017-C-T

180618968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49527983-G-A

180618989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 49527949-C-T

180618999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 49527925-G-A

180618999-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 49527925-G-T

180619140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49527777-T-C

http://identifiers.org/hco/5/GRCh38#180619155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49527762-C-A

180619155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49527762-C-T

http://identifiers.org/hco/5/GRCh38#180619193-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#49527711-C-A

180619193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 49527711-C-T

http://identifiers.org/hco/5/GRCh38#180619199-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#49527674-C-A

180619199-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 49527674-C-G

180619199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 49527674-C-T

180619212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 49527640-G-A

180619212-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 49527640-G-T

180619393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 49527455-G-A

180619393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 49527455-G-T

http://identifiers.org/hco/5/GRCh38#180619399-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49527449-A-C

http://identifiers.org/hco/5/GRCh38#180619447-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49527359-A-C

180619447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49527359-A-G

180619447-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49527359-A-T

180619479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49527327-G-A

180619479-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49527327-G-C

180619479-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49527327-G-T

http://identifiers.org/hco/5/GRCh38#180619484-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49527322-C-A

180619484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49527322-C-T

180619532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49527276-G-A

180619532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49527276-G-T

http://identifiers.org/hco/5/GRCh38#180619533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49527275-C-A

180619533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49527275-C-T

180619535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49527273-T-C

180619539-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49527269-T-A

180619539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49527269-T-C

180619560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49527246-G-T

180619581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49527229-T-C

180619593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49527222-C-T

180619594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49527221-G-A

180619594-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49527221-G-C

180619594-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49527221-G-T

180619654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49527166-T-C

180619821-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49526975-G-T

180619827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49526969-T-C

180619837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49526959-G-T

180619854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49526939-G-A

180619854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49526939-G-T

http://identifiers.org/hco/5/GRCh38#180620122-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49526615-C-A

180620122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49526615-C-T

180620165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 49526570-G-A

180620165-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 49526570-G-T

180620353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49526392-G-T

http://identifiers.org/hco/5/GRCh38#180620386-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49526360-C-A

180620386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49526360-C-T

180620424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49526322-G-A

180620424-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49526322-G-C

180620424-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49526322-G-T

180620451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49526298-C-T

180620474-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49526274-T-G

180620475-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49526273-G-T

180620479-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49526268-G-C

180620479-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49526268-G-T

180620502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49526245-A-G

http://identifiers.org/hco/5/GRCh38#180620510-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49526237-C-A

180620510-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49526237-C-G

180620510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49526237-C-T

180620549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49526193-G-A

180620560-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49526182-T-A

180620560-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49526182-T-G

180620592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49526138-C-T

180620767-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49525959-C-G

180620767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49525959-C-T

180621014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 49525711-G-A

180621014-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 49525711-G-C

180621014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 49525711-G-T

http://identifiers.org/hco/5/GRCh38#180621287-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49525440-C-A

180621319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49525410-G-A

180621319-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49525410-G-T

180621359-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49525381-G-T

180621427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49525276-C-T

180621475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49525244-G-A

180621475-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49525244-G-T

http://identifiers.org/hco/5/GRCh38#180621517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49525205-C-A

180621517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49525205-C-T

180621598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 49525117-A-G

180621625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 49525090-T-C

180621661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 49525054-G-A

180621796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 49524919-C-T

180621958-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49524749-T-G

180621977-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49524730-T-A

180621977-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49524730-T-G

http://identifiers.org/hco/5/GRCh38#180622035-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49524614-C-A

180622035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49524614-C-T

180622085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49524568-G-A

180622359-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49524328-G-C

180622423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49524279-G-A

http://identifiers.org/hco/5/GRCh38#180622610-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49524198-C-A

180622610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49524198-C-T

180622708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49524099-C-T

180622716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49524091-G-A

180622716-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49524091-G-C

180622716-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49524091-G-T

180623044-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49523796-G-T

180623103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49523736-G-A

180623153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 49523671-G-A

180623277-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49523527-T-G

180623784-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49523079-G-T

180623817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49523046-G-A

180623817-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49523046-G-C

180623817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49523046-G-T

180623890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49522960-C-T

180623958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 49522907-C-T

180624135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49522723-G-A

180624135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49522723-G-T

180624151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49522707-G-T

http://identifiers.org/hco/5/GRCh38#180624153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49522705-C-A

180624153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49522705-C-T

180624960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49522326-A-G

180625030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49522258-G-A

180625041-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49522247-T-A

180625041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49522247-T-C

180625041-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49522247-T-G

180625054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49522226-G-A

180625054-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49522226-G-C

180625153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49522113-G-A

180625153-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49522113-G-C

180625998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 49521371-G-A

180626063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49521304-C-T

180626096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49521267-C-T

180626194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 49521165-G-A

180626224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 49521135-T-C

180626277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49521082-A-G

http://identifiers.org/hco/5/GRCh38#180626312-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49521047-C-A

180626312-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49521047-C-G

180626312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49521047-C-T

180627496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49519359-G-A

180627638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49519245-G-A

180627686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49519197-G-A

180628189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49518722-A-G

180628320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49518628-C-T

180628352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49518600-G-A

180628422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49518551-C-T

http://identifiers.org/hco/5/GRCh38#180628615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49518350-C-A

180628620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49518345-C-T

180628657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49518313-G-A

180628657-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49518313-G-C

180628811-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49518118-C-G

180628828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49518101-G-A

180628828-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49518101-G-T

180628840-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49518089-G-T

180628903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 49518041-T-C

180628903-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 49518041-T-G

http://identifiers.org/hco/5/GRCh38#180629073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49517884-C-A

180629073-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49517884-C-G

http://identifiers.org/hco/5/GRCh38#180629152-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49517819-C-A

180629152-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49517819-C-G

180629152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49517819-C-T

180629158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49517813-G-A

180629158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49517813-G-T

http://identifiers.org/hco/5/GRCh38#180629199-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49517774-C-A

180629199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49517774-C-T

180629208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49517765-C-T

180629467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49517454-T-C

http://identifiers.org/hco/5/GRCh38#180629492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49517429-C-A

180629492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49517429-C-T

http://identifiers.org/hco/5/GRCh38#180629519-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49517402-C-A

180629519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49517402-C-T

180629523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49517398-G-A

http://identifiers.org/hco/5/GRCh38#180629565-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49517362-A-C

180629565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49517362-A-G

180629591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49517342-G-A

180629591-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49517342-G-C

180629591-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49517342-G-T

http://identifiers.org/hco/5/GRCh38#180629598-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49517338-C-A

http://identifiers.org/hco/5/GRCh38#180629638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49517303-C-A

180629638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49517303-C-T

180629641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49517300-T-C

180629658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49517283-C-T

180630071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 49516760-A-G

180630093-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 49516738-G-C

180630168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49516699-G-A

180630168-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49516699-G-T

http://identifiers.org/hco/5/GRCh38#180630170-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49516697-C-A

180630170-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49516697-C-G

180630170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49516697-C-T

180630218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 49516642-G-T

180630249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 49516611-G-A

180630249-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 49516611-G-C

180630345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 49516515-G-A

180630345-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 49516515-G-C

180630345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 49516515-G-T

180630431-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49516412-C-G

180630431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49516412-C-T

180630453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49516392-C-T

180630529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49516310-C-T

180630576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 49516275-T-C

180630584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 49516267-G-A

180630646-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 49516205-G-C

180630647-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 49516204-G-C

180630656-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 49516195-T-G

180630721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 49516130-C-T

180630747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 49516104-T-C

180630747-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 49516104-T-G

180630776-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 49516075-G-T

180630794-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 49516057-T-A

http://identifiers.org/hco/5/GRCh38#180630900-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49515947-C-A

180630900-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49515947-C-G

180630900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49515947-C-T

180630901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49515946-C-T

180630915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49515933-G-A

180630915-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49515933-G-T

http://identifiers.org/hco/5/GRCh38#180630929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49515919-C-A

180630929-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49515919-C-G

180630929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49515919-C-T

180631065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49515801-C-T

180631548-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49515705-G-C

180631548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49515705-G-T

180631554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49515699-A-G

180631554-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49515699-A-T

http://identifiers.org/hco/5/GRCh38#180631649-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49515600-C-A

180631649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49515600-C-T

180631760-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 49515488-G-T

180631781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 49515462-G-A

180631781-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 49515462-G-T

180631814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 49515429-T-C

http://identifiers.org/hco/5/GRCh38#180631909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49515334-C-A

180631909-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49515334-C-G

180631909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49515334-C-T

180631940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49515308-G-A

180632127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49515049-A-G

180632168-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49515007-C-G

180632258-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49514953-T-A

180632352-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49514889-T-A

180632459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49514806-G-A

180632627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49514627-T-C

180632635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49514619-T-C

180632657-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49514595-C-G

180632657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49514595-C-T

180632668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49514584-G-A

180632680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49514572-G-A

180632929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49514343-G-A

180632930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49514342-C-T

http://identifiers.org/hco/5/GRCh38#180632989-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49514299-C-A

180633029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49514260-G-A

180633067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49514207-G-A

180633067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49514207-G-T

180633904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49513217-G-A

180634030-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49513119-T-G

180634069-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49513078-T-A

180634262-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49512925-T-A

180639270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49510100-G-A

180639337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49510038-A-G

180639389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49509985-G-A

180639456-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49509926-T-G

180639518-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49509867-G-C

180639521-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49509864-T-G

180639569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49509842-G-A

180639591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49509820-T-C

180639591-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49509820-T-G

180639691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49509719-G-A

180639706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49509684-C-T

180639955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49509438-C-T

180640046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49509346-G-A

180640178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49509234-C-T

180640191-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49509221-C-G

180640405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49509046-G-A

180640423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49509026-C-T

http://identifiers.org/hco/5/GRCh38#180640447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49509003-C-A

180640856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49508528-G-A

180640856-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49508528-G-T

180640868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49508516-C-T

180641036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49508331-C-T

http://identifiers.org/hco/5/GRCh38#180641048-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49508316-C-A

180641048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49508316-C-T

180641138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49508067-G-A

180641507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49507759-C-T

180641665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49507596-G-A

180641707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49507561-G-A

180641735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49507525-C-T

180641737-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49507524-T-A

180641737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49507524-T-C

180641740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49507521-T-C

180641807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49507428-G-T

180641951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49507317-G-A

180641984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49507284-G-A

180642359-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49507155-G-T

180642383-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49507137-T-G

http://identifiers.org/hco/5/GRCh38#180642405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49507115-C-A

180642457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49507089-A-G

180642478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49507068-C-T

180642661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49506918-C-T

180642662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49506917-G-A

180642885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49506697-C-T

180642886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49506696-G-A

180642900-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49506682-G-C

180642906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49506676-G-A

180642916-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49506660-G-T

180643195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49506433-T-C

180643238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49506389-A-G

180643261-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49506365-C-G

180643329-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49506291-G-T

180643351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49506272-C-T

180643368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49506255-A-G

180643640-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49506020-C-G

180643699-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49505952-T-G

180643891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49505840-G-A

http://identifiers.org/hco/5/GRCh38#180643902-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49505832-A-C

180644296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49505689-C-T

180644623-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49505415-T-G

180644633-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49505405-G-T

http://identifiers.org/hco/5/GRCh38#180644802-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49505218-A-C

180644904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 49505119-C-T

180645134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 49504877-G-A

180645134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 49504877-G-T

180645652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49504387-C-T

180645944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49504072-C-T

180645960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49504056-G-A

180645966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49504050-G-A

180645985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49504031-T-C

180646066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49503980-C-T

180646424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49503645-C-T

180646428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49503641-C-T

180646485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49503593-T-C

180646550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49503509-T-C

180646671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49503225-G-A

180646707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49503187-A-G

180646892-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49503051-G-C

http://identifiers.org/hco/5/GRCh38#180647079-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49502899-C-A

180647239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49502774-C-T

http://identifiers.org/hco/5/GRCh38#180647324-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49502698-C-A

180647324-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49502698-C-G

180647324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49502698-C-T

180647410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49502654-G-A

http://identifiers.org/hco/5/GRCh38#180647603-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49502469-C-A

180647603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49502469-C-T

180647622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49502450-G-A

180647925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49502200-G-A

180648318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49501816-G-A

180648512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49501621-C-T

180648543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49501580-C-T

180648683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49501470-C-T

180648729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49501431-C-T

180648819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49501329-C-T

180648843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49501304-C-T

180648909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 49501244-G-T

180649161-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49500961-G-C

180649282-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49500882-G-C

180649345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49500819-C-T

180649439-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49500704-T-A

180649439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49500704-T-C

180649439-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49500704-T-G

180649462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49500683-G-A

180649462-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49500683-G-C

180649462-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49500683-G-T

180649464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49500681-G-A

180649464-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49500681-G-T

http://identifiers.org/hco/5/GRCh38#180649470-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49500665-C-A

180649470-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49500665-C-G

180649470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49500665-C-T

180649562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 49500578-T-C

180649562-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 49500578-T-G

180649574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 49500566-G-A

180649574-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 49500566-G-T

180649575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 49500565-A-G

180649587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 49500553-T-C

http://identifiers.org/hco/5/GRCh38#180649588-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49500552-C-A

180649588-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 49500552-C-G

180649588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 49500552-C-T

180649595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 49500545-G-A

180649595-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 49500545-G-C

180649595-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 49500545-G-T

180649627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron variant
orthologous variants: 49500489-G-A

180649627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron variant
orthologous variants: 49500489-G-T

http://identifiers.org/hco/5/GRCh38#180649712-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49500396-C-A

180649712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron variant
orthologous variants: 49500396-C-T

180649791-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3767
most severe consequence: intron variant
orthologous variants: 49500286-C-G