177087059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55300767-G-A

177087059-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55300767-G-T

177087080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55300787-G-A

177087158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55300854-C-T

177087304-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55301003-G-T

http://identifiers.org/hco/5/GRCh38#177087336-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#55301040-C-A

177087336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55301040-C-T

http://identifiers.org/hco/5/GRCh38#177087401-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#55301106-C-A

177087401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55301106-C-T

177087452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55301137-G-T

177087519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55301192-A-G

177087519-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55301192-A-T

http://identifiers.org/hco/5/GRCh38#177087526-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#55301199-A-C

177087662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55301325-C-T

177087663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55301326-A-G

http://identifiers.org/hco/5/GRCh38#177087675-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#55301333-C-A

177087760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55301414-A-G

177087853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55301487-A-G

177088576-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55302181-G-T

177088940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55302513-G-A

http://identifiers.org/hco/5/GRCh38#177089007-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#55302682-A-C

177089007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55302682-A-G

177089049-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55302744-C-G

177089049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55302744-C-T

177089109-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55302819-A-T

177089154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55302875-T-C

http://identifiers.org/hco/5/GRCh38#177089400-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#55303103-C-A

177089435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55303127-G-A

177089515-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55303198-C-G

177089515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55303198-C-T

177089524-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55303211-G-T

http://identifiers.org/hco/5/GRCh38#177089621-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#55303321-C-A

http://identifiers.org/hco/5/GRCh38#177089811-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#55303481-C-A

177089811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55303481-C-T

http://identifiers.org/hco/5/GRCh38#177090219-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#55303875-C-A

177090219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55303875-C-T

177090245-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55303901-G-T

177090283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55303923-T-C

177090353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55304007-G-A

177090353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55304007-G-T

177090360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55304014-G-A

177090360-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55304014-G-C

177090360-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55304014-G-T

177090478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55304132-T-C

177090591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55304245-G-A

http://identifiers.org/hco/5/GRCh38#177090616-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#55304270-C-A

177090623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55304277-G-A

177091118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55304767-T-C

177091535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55306765-G-A

177091535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55306765-G-T

177091571-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55306801-G-T

http://identifiers.org/hco/5/GRCh38#177091587-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#55306817-C-A

177091587-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55306817-C-G

177091896-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55307126-T-A

177091896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55307126-T-C

177091896-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55307126-T-G

177091934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55307162-G-A

177091934-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55307162-G-T

177091950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55307178-G-A

177091950-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55307178-G-T

177091958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55307186-T-C

http://identifiers.org/hco/5/GRCh38#177091996-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#55307222-A-C

177092022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55307248-G-A

177092054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55307474-C-T

177092245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55307660-G-A

177092245-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55307660-G-T

177092528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55307938-G-A

http://identifiers.org/hco/5/GRCh38#177092545-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#55307955-A-C

http://identifiers.org/hco/5/GRCh38#177092555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#55307977-C-A

177092555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55307977-C-T

177092595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55308015-C-T

177092603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55308022-C-T

177092693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55308109-C-T

177092726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55308142-C-T

177092780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55308196-G-A

177092780-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55308196-G-T

177092858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55308293-G-A

177092858-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55308293-G-T

177092916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55308357-G-A

177092916-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55308357-G-T

177093006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55308539-A-G

177093027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55308580-T-C

177093028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55308581-G-A

177093028-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55308581-G-C

http://identifiers.org/hco/5/GRCh38#177093035-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#55308626-C-A

177093035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55308626-C-T

177093045-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55308696-G-T

http://identifiers.org/hco/5/GRCh38#177093129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#55308920-C-A

177093129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55308920-C-T

177093166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55308957-G-A

177093205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55308996-G-A

177093220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55309011-G-A

177093373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55309175-C-T

http://identifiers.org/hco/5/GRCh38#177093387-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#55309189-C-A

177093387-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55309189-C-G

http://identifiers.org/hco/5/GRCh38#177093441-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#55309242-C-A

177093441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55309242-C-T

177093453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55309254-A-G

177093468-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55309269-C-G

177093483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55309284-C-T

http://identifiers.org/hco/5/GRCh38#177093528-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#55309329-A-C

177093528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 55309329-A-G

177093568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron variant
orthologous variants: 55309363-G-A

177093568-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron variant
orthologous variants: 55309363-G-C

177093568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron variant
orthologous variants: 55309363-G-T

177093571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron variant
orthologous variants: 55309366-G-A

177093631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron variant
orthologous variants: 55309411-G-A

177093631-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron variant
orthologous variants: 55309411-G-C

177094681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron variant
orthologous variants: 55311506-G-A

177094681-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron variant
orthologous variants: 55311506-G-T

http://identifiers.org/hco/5/GRCh38#177094814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#55311679-C-A

177094814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron variant
orthologous variants: 55311679-C-T

http://identifiers.org/hco/5/GRCh38#177095023-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#55311798-C-A

177095023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55311798-C-T

http://identifiers.org/hco/5/GRCh38#177095033-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#55311807-C-A

177095033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55311807-C-T

177095147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55311904-C-T

http://identifiers.org/hco/5/GRCh38#177095156-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#55311913-C-A

177095156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55311913-C-T

177095171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55311927-G-A

177095171-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55311927-G-C

177095171-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55311927-G-T

http://identifiers.org/hco/5/GRCh38#177095196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#55313591-C-A

177095196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55313591-C-T

177095235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55313629-G-A

177095235-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55313629-G-T

177095461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55313832-G-A

177095462-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55313833-C-G

177095462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55313833-C-T

http://identifiers.org/hco/5/GRCh38#177095573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#55313949-C-A

http://identifiers.org/hco/5/GRCh38#177095600-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#55313976-C-A

177095600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: synonymous variant
orthologous variants: 55313976-C-T

177095618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: synonymous variant
orthologous variants: 55313994-C-T

177095621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: synonymous variant
orthologous variants: 55313997-C-T

177095669-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: synonymous variant
orthologous variants: 55314045-G-C

http://identifiers.org/hco/5/GRCh38#177095757-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#55314171-C-A

http://identifiers.org/hco/5/GRCh38#177095769-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#55314210-A-C

177095769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron variant
orthologous variants: 55314210-A-G

177095770-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron variant
orthologous variants: 55314211-C-G

177095770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron variant
orthologous variants: 55314211-C-T

177095791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron variant
orthologous variants: 55314260-A-G

http://identifiers.org/hco/5/GRCh38#177095947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#55314568-C-A

177095968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron variant
orthologous variants: 55314589-G-A

177095968-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron variant
orthologous variants: 55314589-G-C

177095968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron variant
orthologous variants: 55314589-G-T

http://identifiers.org/hco/5/GRCh38#177095978-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#55314597-C-A

177095978-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron variant
orthologous variants: 55314597-C-G

177096225-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron variant
orthologous variants: 55314838-G-C

177096232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron variant
orthologous variants: 55314845-G-A

177096232-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron variant
orthologous variants: 55314845-G-T

177096304-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: missense variant
orthologous variants: 55314918-G-C

177096322-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: synonymous variant
orthologous variants: 55314936-C-G

177096322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: synonymous variant
orthologous variants: 55314936-C-T

177096334-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: synonymous variant
orthologous variants: 55314948-G-T

177096421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron variant
orthologous variants: 55315061-G-A

177096531-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron variant
orthologous variants: 55315134-T-A

177096531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron variant
orthologous variants: 55315134-T-C

177096536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron variant
orthologous variants: 55315139-G-A

177096784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron variant
orthologous variants: 55315385-T-C

http://identifiers.org/hco/5/GRCh38#177096789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#55315390-C-A

177096789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron variant
orthologous variants: 55315390-C-T

177096807-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron variant
orthologous variants: 55315408-C-G

177096807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron variant
orthologous variants: 55315408-C-T

http://identifiers.org/hco/5/GRCh38#177097120-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#55315516-C-A

177097120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron variant
orthologous variants: 55315516-C-T

http://identifiers.org/hco/5/GRCh38#177097121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#55315517-C-A

177097121-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron variant
orthologous variants: 55315517-C-G

177097121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron variant
orthologous variants: 55315517-C-T

http://identifiers.org/hco/5/GRCh38#177097138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#55315534-C-A

177097138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron variant
orthologous variants: 55315534-C-T

http://identifiers.org/hco/5/GRCh38#177097173-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#55315539-A-C

177097173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron variant
orthologous variants: 55315539-A-G

177097173-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron variant
orthologous variants: 55315539-A-T

http://identifiers.org/hco/5/GRCh38#177097226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#55315565-C-A

177097230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55315569-G-A

177097230-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55315569-G-C

177097230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55315569-G-T

177097250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55315583-A-G

177097251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55315584-G-T

177097252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55315585-G-A

177097252-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55315585-G-T

http://identifiers.org/hco/5/GRCh38#177097283-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#55315610-C-A

177097283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55315610-C-T

http://identifiers.org/hco/5/GRCh38#177097324-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#55315651-C-A

177097324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55315651-C-T

177097328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55315655-C-T

177097352-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55315679-G-T

http://identifiers.org/hco/5/GRCh38#177097412-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#55315740-A-C

http://identifiers.org/hco/5/GRCh38#177097415-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#55315744-C-A

177097415-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55315744-C-G

177097415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55315744-C-T

177097432-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55315761-T-A

177097432-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55315761-T-G

177097670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55315982-G-A

177097685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 55316001-C-T

177097689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 55316005-G-A

177097689-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 55316005-G-C

177097689-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 55316005-G-T

177097698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 55316014-G-A

http://identifiers.org/hco/5/GRCh38#177097721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#55316037-C-A

http://identifiers.org/hco/5/GRCh38#177097802-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#55316117-C-A

http://identifiers.org/hco/5/GRCh38#177097836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#55316156-C-A

177097836-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: 3 prime UTR variant
orthologous variants: 55316156-C-G

177097836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: 3 prime UTR variant
orthologous variants: 55316156-C-T

177097893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: 3 prime UTR variant
orthologous variants: 55316292-T-C

177097893-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: 3 prime UTR variant
orthologous variants: 55316292-T-G

http://identifiers.org/hco/5/GRCh38#177097906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#55316306-C-A

177097906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: 3 prime UTR variant
orthologous variants: 55316306-C-T

177097916-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: 3 prime UTR variant
orthologous variants: 55316316-T-A

177097916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: 3 prime UTR variant
orthologous variants: 55316316-T-C

http://identifiers.org/hco/5/GRCh38#177097920-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#55316320-C-A

177097920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: 3 prime UTR variant
orthologous variants: 55316320-C-T

http://identifiers.org/hco/5/GRCh38#177097925-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#55316325-C-A

177097925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: 3 prime UTR variant
orthologous variants: 55316325-C-T

177097977-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: 3 prime UTR variant
orthologous variants: 55316379-T-A

177097977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: 3 prime UTR variant
orthologous variants: 55316379-T-C

177097978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: 3 prime UTR variant
orthologous variants: 55316380-G-A

177097978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: 3 prime UTR variant
orthologous variants: 55316380-G-T

http://identifiers.org/hco/5/GRCh38#177097989-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#55316391-C-A

177097989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: 3 prime UTR variant
orthologous variants: 55316391-C-T

http://identifiers.org/hco/5/GRCh38#177097993-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#55316406-C-A

177098068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: 3 prime UTR variant
orthologous variants: 55316492-T-C

177098069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: 3 prime UTR variant
orthologous variants: 55316493-G-A

177098069-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: 3 prime UTR variant
orthologous variants: 55316493-G-T

177098077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: 3 prime UTR variant
orthologous variants: 55316501-G-A

177098077-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: 3 prime UTR variant
orthologous variants: 55316501-G-C

177098077-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3691
most severe consequence: 3 prime UTR variant
orthologous variants: 55316501-G-T